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Learn MoreTopical minoxidil is the most established over-the-counter treatment for hair loss, with decades of use behind its FDA approval. But how does it actually work, and what determines whether it will work for you? In this article, we explore the science behind topical minoxidil, its strengths and limitations, key factors that influence its success, how to enhance results with add-ons like microneedling or retinoids, and what to expect over the course of months and years of use.
Topical minoxidil is one of the most widely used treatments for hair loss, known for its accessibility, relatively low risk profile, and ability to slow or partially reverse androgenetic alopecia in both men and women. First developed as a blood pressure medication, it gained FDA approval in the 1980s after researchers observed its unexpected side effect, stimulating hair growth when applied to the scalp.
In this article, we examine the mechanisms of action, formulation differences, dosing strategies, long-term efficacy, side effects, and methods to enhance results through combination therapies, such as microneedling or retinoids. Whether you’re just starting your hair restoration journey or reassessing your regimen, this guide provides an evidence-based foundation to help you make informed decisions.
Topical minoxidil formulations were originally developed in the early 1980s after an interesting side effect was discovered when it was used as an oral hypertensive agent. This side effect was hypertrichosis, or increased hair growth. The U.S. FDA approved topical minoxidil for male pattern hair loss in 1988 and for female pattern hair loss in 1991.[1]Suchonwanit, P., Thammarucha, S., Leerunyakul, K. (2019). Minoxidil and its use in hair disorders: a review. Drug Design, Development and Therapy. 13. 2777-2786. Available at: … Continue reading
Minoxidil is a pro-drug: it requires enzymatic activation to exert its pharmacological effect on hair follicles. The key enzyme involved in this is sulfotransferase SULT1A1, which is highly expressed in the outer root sheath (ORS) of hair follicles.[2]Bacqueville, D., Jacques, C., Duprat, L., Jamin, E.L., Guiraud, B., Perdu, E., Bessou-Touya, S., Zalko, D., Duplan, H. (2017). Characterization of xenobiotic metabolizing enzymes of a reconstructed … Continue reading The level of SULT1A1 activity in the hair follicle correlates strongly with clinical response to topical minoxidil; individuals with low SULT1A1 activity are less likely to benefit from treatment.[3]Pietrauszka, K., Bergler-Czop, B. (2020). Sulfotransferase SULT1A1 activity in hair follicle, a prognostic marker of response to the minoxidil treatment in patients with androgenetic alopecia: a … Continue reading
Topical minoxidil typically comes in two main formulations:
Some options also offer propylene glycol-free solutions and gels. Some newer products use water-based or liposomal vehicles to cater to users with sensitive skin or allergies.
Many people opt for topical minoxidil over oral formulations due to key differences in safety, accessibility, and side effect profiles.
Topical minoxidil is available over the counter, making it easy to obtain and start treatment promptly. Oral minoxidil, however, requires a prescription and is typically used off-label for hair loss, which can delay access and introduce hurdles within the healthcare system.
Applying minoxidil directly to the scalp results in minimal absorption into the bloodstream. This localized delivery reduces the risk of systemic side effects that are more common with oral minoxidil, which circulates throughout the body.[6]Ashique, S., Sandhu, N.K., Haque, S.N., Koley, K. (2020). A Systemic Review on Topical Marketed Formulations, Natural Products, and Oral Supplements to Prevent Androgenic Alopecia: A Review. Natural … Continue reading
Oral minoxidil demonstrates a high incidence of hypertrichosis, whereas in topical minoxidil, it is usually localized and linked to misuse.[7]Jiminez-Cauhe, J., Sicco, K.I.L., Shapiro, J., Hermosa-Gelbard, A., Burgos-Blasco, P., Melian-Olivera, A., Ortega-Quijano, D., Pindado-Ortega, C., Buendia-Castano, D., Asz-Sigall, D., Vano-Galvan, S. … Continue reading
Similarly, edema (fluid retention/swelling) and cardiac side effects (such as tachycardia, pericardial effusion, and exacerbation of angina) are rare with topical use but do have the potential to cause issues for those with preexisting cardiovascular, renal, or hepatic conditions.[8]do Nascimento, I.J.B., Harries, M., Rocha, V.B., Thompson, J.Y., Wong, C.H., Varkaneh, H.K., Guimaraes, N.S., Arantes, A. J. R., Marcolini, M.S. (2020). Effect of Oral Minoxidil for Alopecia: … Continue reading
Topical minoxidil stimulates hair growth through a variety of interconnected biological mechanisms, many of which have been elucidated in peer-reviewed research.
Minoxidil acts as a potent vasodilator by opening potassium channels in vascular smooth muscle, leading to increased blood flow around hair follicles. This enhanced microcirculation delivers more oxygen and nutrients to the follicular environment, creating conditions favorable for hair growth.
Additionally, minoxidil upregulates the expression of vascular endothelial growth factor (VEGF) in dermal papilla cells. VEGF is a key mediator of angiogenesis, supporting the development and maintenance of the follicular blood supply necessary for robust hair growth.[9]Zeltzer, A.A., Keren, A., Paus, R., Gilhar, A. (2024). Topical minoxidil rejuvenates hair follicles from men with androgenetic alopecia in vivo. Acta Dermato Venereologica. 104(24213). Available at: … Continue reading
One of the hallmark effects of topical minoxidil is its ability to induce the anagen (growth) phase of the hair cycle and shorten the telogen (resting) phase.[10]Van Neste, D. (2020). Placebo-controlled dose-effect studies with topical minoxidil 2% or 5% in male-patterned hair loss treated with oral finasteride employing an analytical and exhaustive study … Continue reading By prompting resting hair follicles to re-enter the growth phase more rapidly, minoxidil effectively “resets” the hair cycle, leading to increased hair density and thickness over time. This is a central reason for its clinical efficacy in treating AGA and other hair loss disorders.
Recent studies have shown that minoxidil activates the Wnt/ꞵ-catenin signaling pathway within dermal papilla cells. This pathway is essential for hair follicle development, regeneration, and maintenance. Activation of ꞵ-catenin dermal papilla cells prolongs the anagen phase and supports the proliferation and differentiation of follicular cells, further enhancing hair growth.[11]Kwack, M.H., Kang, B.M., Kim, M.K., Kim, J.C., Sung, Y.K. (2011). Minoxidil activates ꞵ-catenin pathway in human dermal papilla cells: a possible explanation for its anagen prolongation effect. … Continue reading
Minoxidil has been found to increase the production of prostaglandin E2 (PGE2) by activating prostaglandin synthase-1 (PGHS-1) in dermal papilla fibroblasts. Elevated PGE2 levels are associated with hair growth promotion, possibly by providing cytoprotective effects and modulating local inflammation within the follicle environment.[12]Michelet, J.F., Commo, S., Billoni, N., Mahe, Y.F., Bernard, B.A. (1997). Activation of cytoprotective prostaglandin synthase-1 by minoxidil as a possible explanation for its hair growth-stimulating … Continue reading This prostaglandin modulation may also counteract the inhibitory effects of certain nonsteroidal anti-inflammatory drugs (NSAIDs).
The effectiveness of topical minoxidil depends significantly on its ability to penetrate the scalp and reach the hair follicle. Only about 1.4% of applied minoxidil is typically absorbed through intact skin.[13]Gupta, A.K., Talukder, M., Venkataraman, M., Bamimore, M.A. (2022). Minoxidil: a comprehensive review. Journal of Dermatological Treatment. 33(4). 1896-1906. Available at: … Continue reading
The formulation’s vehicle (e.g., alcohol-based solution, foam, or novel delivery systems like cetosomes), the integrity of the skin barrier (stratum corneum), and the presence of activating enzymes (notably sulfotransferase SULT1A1 in the outer root sheath) all influence absorption and efficacy.[14]Sattur, S. Talathi, A., Shetty, G., Arsiwala, S., Pereira, R., Dhoot, D. (2023). Comparative Clinical Study Evaluating the Efficacy and Safety of Topical 5% Cetosomal Minoxidil and Topical 5% … Continue reading
Clinical studies have demonstrated that once-daily application of 5% topical minoxidil achieves hair count improvements comparable to twice-daily use of the 2% solution in men with AGA.[15]Olsen, E.A., Dunlap, F.E., Funicella, T., Koperski, J.A., Swinehart, J.M., Tschen, E.H., Trancik, R.J. (2002). A randomized clinical trial of 5% topical minoxidil versus 2% topical minoxidil and … Continue reading In long-term studies, men who switched from twice daily to once-daily minoxidil maintained most of their hair gains, though there was a slightly greater mean loss in those on the once-daily regimen compared to those who remained on twice-daily dosing.[16]Olsen, E.A., DeLong, E.R., Weiner, M.S. (1987). Long-term follow-up of men with male pattern baldness treated with topical minoxidil. Journal of the American Academy of Dermatology. 16(3 Pt 2). … Continue reading
Importantly, using 5% minoxidil twice daily can provide an incremental benefit, approximately 10-15% greater hair regrowth, over once-daily 5% application or twice-daily 2% solution, though this comes with a higher risk of local irritation.[17]Olsen, E.A., Dunlap, F.E., Funicella, T., Koperski, J.A., Swinehart, J.M., Tschen, E.H., Trancik, R.J. (2002). A randomized clinical trial of 5% topical minoxidil versus 2% topical minoxidil and … Continue reading
For women with FPHL, randomized clinical trials have shown that once-daily application of 5% minoxidil foam is non-inferior to twice-daily use of the 2% minoxidil solution in terms of hair regrowth and target area hair counts.[18]Blume-Peytavi, U., Hillmann, K., Dietz, E., Canfield, D., Bartels, N.G. (2011). A randomized, single-blind trial of 5% minoxidil foam once daily versus 2% minoxidil solution twice daily in the … Continue reading Both regimens lead to similar improvements, but the once-daily 5% foam offers a significant compliance advantage, as it is easier to incorporate into daily routines and is associated with fewer reports of scalp irritation.[19]Ramos, P.M., Melo, D.F., Radwanski, H., de Almeida, R.F.C., Miot, H.A. (2023). Female-pattern hair loss: therapeutic update. Anais Brasileiros de Dermatologica. 98(4). 506-519. Available at: … Continue reading This practical benefit makes once-daily 5% foam a preferred initial therapy for many women.
Selecting the right minoxidil concentration depends on your goals, tolerance, and clinical context.
There are a number of options you can take in terms of formulation or additional treatments to improve the efficacy of topical minoxidil.
Liquid minoxidil formulations can contain propylene glycol, which improves drug solubility and skin penetration.[25]Grice, J.E., Ciotti, S., Weiner, N., Lockwood, P., Cross, S.E., Roberts, M.S. (2010). Relative uptake of minoxidil into appendages and stratum corneum and permeation through human skin in vitro. … Continue reading However, propylene glycol is a frequent cause of scalp irritation; itching, redness, and flaking are common complaints, especially among users with sensitive skin.[26]Patel, K., Palmer, A., Nixon, R. (2023). Allergic contact dermatitis from propylene glycol: A case series from Australia. Contact Dermatitis. 89(2). 79-84. Available at: … Continue reading
Foam minoxidil was specifically developed to avoid propylene glycol usage and minimize irritation. As a result, foam is generally much better tolerated, especially for individuals prone to dermatitis or scalp discomfort.[27]Nestor, M.S., Ablon, G., Gade, A., Han, H., Fischer, D.L. (2021). Treatment options for androgenetic alopecia: Efficacy, side effects, compliance, financial considerations, and ethics. Journal of … Continue reading Additionally, the foam dries faster than the traditional liquid, making it more convenient for daily use.
Efficacy: Most comparative studies and clinical experience suggest the 5% foam and 2% liquid are equivalent in hair regrowth when used appropriately; the choice often comes down to scalp tolerance and application preference.[28]Blume-Peytavi, U., Hillmann, K., Dietz, E., Canfield, D., Bartels, N.G. (2011). A randomized, single-blind trial of 5% minoxidil foam once-daily versus 2% minoxidil solution twice daily in the … Continue reading
For patients unable to tolerate propylene glycol or those seeking even less greasy, faster-drying options, newer propylene glycol-free formulations have been developed. These often use other solvents or humectants, with in vitro and clinical studies showing similar efficacy to products containing propylene glycol.[29]Barbareschi, M., Vescovi, V., Starace, M., Piraccini, B.M., Milani, M. (2020). Propylene glycol free 5% minoxidil lotion formulation: cosmetic acceptability, local tolerability, clinical efficacy and … Continue reading
As mentioned above, SULT1A1 is the key enzyme in the hair follicle that activates minoxidil by converting it to minoxidil sulfate, its effective form. Retinoids, notably tretinoin (0.01-0.025%), can be added to topical regimens to upregulate SULT1A1 in the outer root sheath, enhancing the local activation of minoxidil.[30]Sharma, A., Goren, A., Dhurat, R., Agrawal, S., Sinclair, R., Trueb, R.M., Vano-Galvin, S., Chen, G., Tan, Y., Kovacevic, M., Situm, M., McCoy, J. (2019). Tretinoin enhances minoxidil response in … Continue reading
The mechanism appears to involve both increased skin permeability and direct modulation of SULT1A1 gene expression, making this combination particularly useful for patients with known or suspected low enzyme activity.
When assessing the benefits of topical minoxidil, it’s critical to consider how response rates, regrowth rates, and especially months of use influence real-world outcomes for individuals with AGA. While many early studies highlight minoxidil’s promise, longer-term data reveal a more nuanced reality.
Within 3-6 months, minoxidil demonstrates high response rates. Surveys and clinical studies consistently show that roughly 60% of men perceive a meaningful response (slowing, stopping, or reversal of hair loss) in this window (as per self-assessment and investigator evaluations).[31]Asilian, A., Farmani, A., Saber, M. (2023). Clinical efficacy and safety of low-dose oral minoxidil versus topical solution in the improvement of androgenetic alopecia: A randomized controlled trial. … Continue reading
After one year or longer, response rates drop dramatically. Multiple studies report rates below 30%, and even lower in five-year follow-up populations, with only about 20-30% of users satisfied with the results.[32]Olsen, E.A., Weiner, M.S., Amara, I.A., DeLong, E.R. (1990). Five-year follow-up of men with androgenetic alopecia treated with topical minoxidil. Journal of American Academy of Dermatology. 22(4). … Continue reading
Real-world data indicate discontinuation rates of 86–95% by the one-year mark. The leading reason cited by users for stopping? “Low effect,” or disappointment with the cosmetic improvement offered by the drug.[33]Shadi, Z. (2023) Compliance to Topical Minoxidil and Reasons for Discontinuation among Patients with Androgenetic Alopecia. Dermatology and Therapy. 13(5). 1157-1169. Available at: … Continue reading
In one pivotal trial, men using 5% minoxidil twice daily saw a nearly 60% increase in hair “weight” (total mass of regrown/thickened hair) at 6 months. By 96 weeks, gains had diminished to just 25% above the baseline, a significant drop from the initial response.[34]Van Neste, D. (2020). Placebo-controlled dose-effect studies with topical minoxidil 2% or 5% in male-patterned hair loss treated with oral finasteride employing an analytical and exhaustive study … Continue reading
Over 48 weeks, users displayed a 12% rise in hair count compared with 3% for placebo (statistically significant). Still, these increases in hair number did not always correspond to better visible scalp coverage when judged by experts, indicating that raw hair counts may overstate clinical benefit.
Lack of DHT Targeting and Ongoing Miniaturization
Minoxidil’s primary action is to stimulate hair follicles into a growth (anagen) phase; however, it does not block the effects of DHT, the androgen responsible for follicle miniaturization in genetic hair loss.[35][Updated 2023 Feb 24]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK482378/ Accessed: July 2025 Therefore, hair shafts may still become thinner despite greater numbers, diminishing real-world cosmetic impact.
Fibrosis: The Hidden Limitation
Emerging evidence points to fibrosis, the gradual formation of restrictive, scar-like tissue around miniaturizing follicles, as a rate-limiting factor in AGA.[36]Trueb, R.M., Dias, M.F.R.G., Rezende, H.D. (2021). Comment on Follicular Inflammation and Fibrosis in Pattern Hair Loss. Skin Appendage Disorders. 7(2). 159-160. Available at: … Continue reading Minoxidil does not directly address this fibrotic process, so even if follicles are nudged back into growth, their ability to produce robust hair continues to decline as surrounding tissue stiffens and shrinks.
The Limits of Hair Count as a Metric
Statistical increases in hair count do not guarantee clinical satisfaction. Studies repeatedly show that even impressive numeric gains in hair counts (or surrogate measures, such as hair mass index) are not always matched by noticeable differences in scalp coverage or user satisfaction.[37]Van Neste, D. (2020). Placebo-controlled dose-effect studies with topical minoxidil 2% or 5% in male-patterned hair loss treated with oral finasteride employing an analytical and exhaustive study … Continue reading Patient dissatisfaction and discontinuation remain high in the absence of true visual improvement, underscoring the practical limits of relying on surrogate endpoints.
Recent clinical trials have shown that adding microneedling to minoxidil treatment can significantly enhance both response and regrowth rates. One landmark study reported a nearly fourfold greater increase in hair count (approximately a 40% gain) compared to minoxidil alone at 12 weeks, with participants experiencing actual visible improvements in density.[38]Ahmed, K.M.A., Kozaa, Y.A., Abuawwad, M.T., Al-Najdawi, A.I.A., Mahmoud, Y.W., Ahmed, A.M., Taha, M.J.J., Fadhli, T., Giannopoulou, A. (2025). Evaluating the efficacy and safety of combined … Continue reading
A six-month trial showed an 85% effective rate and a significant increase in hair count for the combination approach.[39]Zhang, Y., Sheng, Y., Zeng, Y., Hu, R., Zhao, J., Wang, W., Yang, Q. (2022). Randomized trial of microneedling combined with 2% minoxidil topical solution for the treatment of female pattern hair … Continue reading
Figure 1: A 35-year-old female patient with 5 years of FPHL in group 2 (combination treatment) at baseline and endline.[40]Zhang, Y., Sheng, Y., Zeng, Y., Hu, R., Zhao, J., Wang, W., Yang, Q. (2022). Randomized trial of microneedling combined with 2% minoxidil topical solution for the treatment of female pattern hair … Continue reading
For people who don’t respond adequately to topical minoxidil, several strategies can help overcome this resistance and optimize hair growth.
Raising the concentration of topical minoxidil beyond 5%, to compounded strengths such as 7% or 10%, is a common clinical approach for patients identified as poor responders. The rationale is that higher drug levels may compensate, at least partially, for suboptimal enzymatic conversion of minoxidil to its active sulfate form in the outer root sheath.
Topical retinoic acid (such as tretinoin) can be combined with minoxidil to upregulate SULT1A1 activity, thereby enhancing the local activation of minoxidil in the hair follicle. Peer-reviewed research indicates that applying topical tretinoin upregulates follicle sulfotransferase enzymes, thereby enhancing the response to minoxidil.[42]Sharma, A., Goren, A., Dhurat, R., Agrawal, S., Sinclair, R., Trueb, R.M., Vano-Galvan, S., Chen, G., Tan, Y., Kovacevic, M., Situm, M., McCoy, J. (2019). Tretinoin enhances minoxidil response in … Continue reading
Microneedling is an increasingly popular adjunctive treatment for hair loss, particularly in individuals who do not respond to minoxidil. Weekly sessions using devices with needles 0.5–1.5 mm in length create controlled micro-injuries in the scalp, stimulating growth factors, activating dermal papilla cell signaling (such as Wnt/β-catenin), and boosting SULT1A1 enzyme expression.[43]Dhurat, R., Sukesh, M.S., Avhad, G., Dandale, A., Pal, A., Pund, P. (2013). A Randomized Evaluator Blinded Study of Effect of Microneedling in Androgenetic Alopecia: A Pilot Study. International … Continue reading,[44]Kumar, K.M., Inamadar, A.C., Palit, A. (2018). A Randomized Controlled, Single-Observer Blinded Study to Determine the Efficacy of Topical Minoxidil plus Microneedling versus Topical Minoxidil Alone … Continue reading,[45]Zhang, Y., Sheng, Y., Zeng, Y., Hu, R., Zhao, J., Wang, W., Yang, Q. (2022). Randomized trial of microneedling combined with 2% minoxidil topical solution for the treatment of female pattern hair … Continue reading
Low-dose oral minoxidil, typically 0.25–5 mg daily, offers systemic activation, as minoxidil is converted to its active sulfate in the liver (where SULT1A1 levels are abundant).[46]Ramirez-Marin, H.A., Tosti, A. (2022). Role of Oral Minoxidil in Patterned Hair Loss. Indian Dermatology Online Journal. 13(6). 729-733. Available at: https://doi.org/10.4103/idoj.idoj_246_22 For individuals whose follicular SULT1A1 is insufficient for topical efficacy, oral minoxidil can bypass the need for high local enzyme activity. Recent comprehensive reviews and clinical experience suggest that low-dose oral minoxidil is effective for hair regrowth in male and female pattern hair loss, with a favorable safety profile when started at low dosages.[47]Gupta, A.K., Talukder, M., Shemer, A., Piraccini, B.M., Tosti, A. (2023). Low-Dose Oral Minoxidil for Alopecia: A Comprehensive Review. Skin Appendage Disorders. 9(6). 423-437. Available at: … Continue reading
Compounding pharmacies can prepare topical formulations containing minoxidil sulfate, the direct, active metabolite, bypassing the need for SULT1A1 conversion. Though theoretically attractive for SULT1A1 nonresponders, minoxidil sulfate is chemically less stable than parent minoxidil and is also more expensive.[48]Chemical Book. (no date). Minoxidil Sulphate. ChemBook. Available at: https://www.chemicalbook.com/Price/Minoxidil-sulphate.htm Accessed: July 2025,[49]Shan, Y., Xu, C., Guo, Y., Wen, L., Zhou, S., Fang, L., Xu, J., Zhen, H. (2025). Liposomes enhance the hair follicle delivery of minoxidil sulfate with improved treatment of androgenetic alopecia. … Continue reading Its shelf-life, risk of degradation, and limited availability currently constrain its widespread clinical use. Efficacy and safety data are lacking beyond case reports and experimental settings, and this approach remains investigational.
Understanding the typical milestones and changes during minoxidil treatment helps set realistic expectations, avoids premature discontinuation, and guides regimen adjustments for optimal hair regrowth. Here’s a week-by-week and month-by-month breakdown based on clinical evidence and peer-reviewed research.
What happens: Many users notice an initial increase in hair shedding after starting minoxidil, usually peaking around weeks 4–6.
Why: This effect, known as telogen effluvium, occurs as minoxidil accelerates the transition of hair follicles from the resting (telogen) to the active (anagen) growth phase. Older, miniaturized hairs are shed to make way for new ones.
What to do: This shedding is temporary and generally indicates that the treatment is starting to take effect. Stopping minoxidil because of early shedding is unnecessary and may forfeit later gains.
What happens: Fine, soft “vellus” hairs begin to thicken. With combination treatments (such as minoxidil plus microneedling), these changes may be more pronounced and start to become cosmetically noticeable.
Why: Follicles kickstart new anagen cycles, and some can already be seen transitioning to more pigmented, visible hairs.[50]Rafi, A.W., Katz, R.M. (2011). Pilot study of 15 patients receiving a new treatment regimen for androgenic alopecia: the effects of atopy on AGA. ISRN Dermatology. 11. 241953. Available at: … Continue reading
Expectations: While cosmetic gains are modest at this stage using monotherapy, up to 60–74% of users report improvement in density and coverage when asked at 3–4 months.[51]Rundegren, J. (2004). Rapid onset of action of minoxidil 5% topical solution in a 4-month German observational study on both patients and physicians. Journal of the American Academy of Dermatology. … Continue reading
What happens: The majority of the visible thickening and coverage improvements emerge by 6-8 months. Around this time, many people also see gains plateau and further visible regrowth slows considerably
Clinical evidence: At this point, studies show peak increases in terminal hair count and density (e.g., a 12–15% rise for standard 5% twice-daily solutions in men).[52]Olsen, E.A., Dunlap, F.E., Funicella, T., Koperski, J.A., Swinehart, J.M., Tschen, E.H., Trancik, R.J. (2002). A randomized clinical trial of 5% topical minoxidil versus 2% topical minoxidil and … Continue reading
What to do: Regimen reevaluation is appropriate here; ensure ongoing compliance, assess satisfaction, and consider any adjuncts or boosters if progress is suboptimal. If additional improvement is desired, this is the window to explore adjunctive approaches, such as adding microneedling, retinoids, or anti-androgen therapies, to enhance or sustain growth.
What happens: Many users see diminishing improvements after 9 months; some may even experience slow retreating benefits despite continued use.
Why: Minoxidil alone does not address the underlying drivers of androgenetic alopecia, namely, DHT-mediated follicle miniaturization and progressive perifollicular fibrosis. Without combining minoxidil with anti-DHT agents or regenerative wounding therapies, natural progression often limits sustained gains.
Long-term evidence: Only ~30% of users report being satisfied after several years; discontinuation is common, with the lack of a visible effect being the primary reason.[53]Shadi, Z. (2023) Compliance to Topical Minoxidil and Reasons for Discontinuation among Patients with Androgenetic Alopecia. Dermatology and Therapy. 13(5). 1157-1169. Available at: … Continue reading
Discontinuing topical minoxidil is a significant decision, as virtually all clinical evidence and real-world experience indicate that hair gains made during treatment will be lost, usually within 3 to 12 months. This process is driven by the underlying physiology of follicles and the progressive nature of AGA.
One 96-week study on both 2% and 5% topical minoxidil found that after treatment was halted, hair counts and weight fell below both baseline and placebo levels within 3 months.[58]Price, V.H., Menefee, E., Strauss, P.C. (1999). Changes in hair weight and hair count in men with androgenetic alopecia, after application of 5% and 2% topical minoxidil, placebo, or no treatment. … Continue reading By six months post-withdrawal, most subjects’ hair counts rebounded to baseline, indicating the temporary and reversible effects of minoxidil therapy in AGA.
Figure 2: Comparison of mean percentage change in interval weight per square centimeter for 4 treatment groups. Vertical line at 96 weeks marks cessation of treatment.[59]Price, V.H., Menefee, E., Strauss, P.C. (1999). Changes in hair weight and hair count in men with androgenetic alopecia, after application of 5% and 2% topical minoxidil, placebo, or no treatment. … Continue reading
Abruptly ceasing minoxidil use (“cold turkey”) tends to induce more severe and acute shedding. To mitigate this shock to the hair cycle and scalp, expert opinion and clinical guidelines recommend a gradual taper, similar to protocols used for oral minoxidil or other hair loss medications.
A 6-month Tapering Schedule could look like this.
Weeks | Protocol Description |
1-2 | Alternate once-daily and twice-daily applications |
3-4 | Three days once-daily, one day twice-daily |
5-6 | Once daily, Monday-Friday, twice on weekends |
7-9 | Once daily |
10-12 | Once daily on weekdays, off weekends |
13-15 | Once daily, Monday-Thursday, off Friday-Sunday |
16-18 | Apply every other day |
19 | Every third day |
20 | Every fourth day |
21 | Every fifth day |
22 | Every sixth day |
23 | Once weekly, then discontinue |
No protocol can eliminate post-minoxidil shedding, but supporting the scalp with additional therapies may enhance retention and cushion the transition.
You can read our article on what happens when you quit taking minoxidil here.
You’re a good candidate if you are:
Who May Want to Reconsider?
Will minoxidil lower my libido? No, minoxidil is not known to lower libido, as it does not affect hormones and has shown no significant link to sexual side effects in clinical studies or post-marketing data. For more information, refer to the following resources: Minoxidil: Getting Started (Interactive Guide).
Can I dilute topical minoxidil without losing its efficacy? You can dilute topical minoxidil or mix it with other topicals, but doing so may reduce its efficacy if it alters absorption, concentration, or stability, so it’s best to either separate applications (morning vs. evening) or use professionally compounded combinations to ensure reliable results. For more information, watch this video.
Can I use topical minoxidil alongside other topicals? Yes, you can use topical minoxidil alongside other topicals, but to avoid interference with absorption, it’s best to either apply them at different times of day (e.g., morning vs. evening) or combine them into a single formulation, ideally through a compounding pharmacy or by carefully preparing them at home following best practices.
How long should I leave minoxidil on my scalp? You should leave minoxidil on your scalp for at least one hour, but ideally for four hours or more, to ensure optimal absorption, especially if you’re applying it only once a day. Most of the drug is absorbed within the first few hours, so extending contact time helps maximize its effectiveness.
Does minoxidil accelerate skin aging? Minoxidil is unlikely to accelerate skin aging; reported changes in facial skin quality are more likely due to mild allergic reactions to propylene glycol or temporary water retention, both of which are typically reversible and manageable with formulation changes or improved application practices.
Topical minoxidil remains the cornerstone over‑the‑counter therapy for androgenetic alopecia, valued for its solid safety record, ease of access, and decades of clinical data supporting meaningful, if often modest, improvements in hair density and retention. For many men and women, especially those early in their hair-loss journey or those averse to systemic medications, it offers a practical first line of defense that can be further amplified with adjuncts such as microneedling, retinoids, or anti-androgens.
Yet its benefits are not limitless: results plateau without complementary treatments, lifelong use is required to maintain gains, and irritation or simple user fatigue remain common reasons for discontinuation. Approached realistically, committing to at least six months of consistent, correctly dosed application, monitoring scalp health, and integrating synergistic therapies where appropriate, topical minoxidil can serve as a reliable, evidence‑based pillar in a comprehensive hair‑restoration plan.
References[+]
↑1 | Suchonwanit, P., Thammarucha, S., Leerunyakul, K. (2019). Minoxidil and its use in hair disorders: a review. Drug Design, Development and Therapy. 13. 2777-2786. Available at: https://doi.org/10.2147/DDDT.S214907 |
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↑2 | Bacqueville, D., Jacques, C., Duprat, L., Jamin, E.L., Guiraud, B., Perdu, E., Bessou-Touya, S., Zalko, D., Duplan, H. (2017). Characterization of xenobiotic metabolizing enzymes of a reconstructed human epidermal model from adult hair follicles. Toxicology and Applied Pharmacology. 15(329). 190-201. Available at: https://doi.org/10.1016/j.taap.2017.05.040 |
↑3 | Pietrauszka, K., Bergler-Czop, B. (2020). Sulfotransferase SULT1A1 activity in hair follicle, a prognostic marker of response to the minoxidil treatment in patients with androgenetic alopecia: a review. Advances in Dermatology and Allergology. 39(3). 472-478. Available at: https://doi.org/10.5114/ada.2020.99947 |
↑4 | Epstein, G.K., Epstein, J., Cohen, J. (2019). Hair Loss in Men and Women: Medical and Surgical Therapies. 2(1). 161-176. Available at: https://doi.org/10.1016/j.yacs.2019.02.006 |
↑5 | Lupatini, R., Sidhu, R., Patel, H., Bichar, K. (2021). Stability Evaluation of Minoxidil in FOAMIL Foam Base with Bracketing Study Design. International Journal of Pharmaceutical Compounding. 25(3) 236-240. Available at: PMID: 34125714 |
↑6 | Ashique, S., Sandhu, N.K., Haque, S.N., Koley, K. (2020). A Systemic Review on Topical Marketed Formulations, Natural Products, and Oral Supplements to Prevent Androgenic Alopecia: A Review. Natural Products and Bioprospecting. 10(6). 345-365. Available at: https://doi.org/10.1007/s13659-020-00267-9 |
↑7 | Jiminez-Cauhe, J., Sicco, K.I.L., Shapiro, J., Hermosa-Gelbard, A., Burgos-Blasco, P., Melian-Olivera, A., Ortega-Quijano, D., Pindado-Ortega, C., Buendia-Castano, D., Asz-Sigall, D., Vano-Galvan, S. (2025). Characterization and Management of Adverse Events of Low-Dose Oral Minoxidil Treatment for Alopecia: A Narrative Review. Journal of Clinical Medicine. 14(6). 1805. Available at: https://doi.org/10.3390/jcm14061805 |
↑8 | do Nascimento, I.J.B., Harries, M., Rocha, V.B., Thompson, J.Y., Wong, C.H., Varkaneh, H.K., Guimaraes, N.S., Arantes, A. J. R., Marcolini, M.S. (2020). Effect of Oral Minoxidil for Alopecia: Systematic Review. International Journal of Trichology. 12(4). 147-155. Available at: https://doi.org/10.4103/ijt.ijt_19_20 |
↑9 | Zeltzer, A.A., Keren, A., Paus, R., Gilhar, A. (2024). Topical minoxidil rejuvenates hair follicles from men with androgenetic alopecia in vivo. Acta Dermato Venereologica. 104(24213). Available at: https://doi.org/10.2340/actadv.v104.24213 |
↑10 | Van Neste, D. (2020). Placebo-controlled dose-effect studies with topical minoxidil 2% or 5% in male-patterned hair loss treated with oral finasteride employing an analytical and exhaustive study protocol. Skin Research and Technology. 26(4). 542-557. Available at: https://doi.org/10.1111/srt.12827 |
↑11 | Kwack, M.H., Kang, B.M., Kim, M.K., Kim, J.C., Sung, Y.K. (2011). Minoxidil activates ꞵ-catenin pathway in human dermal papilla cells: a possible explanation for its anagen prolongation effect. Journal of Dermatological Science. 154-159. Available at: https://doi.org/10.1016/j.jdermsci.2011.01.013 |
↑12 | Michelet, J.F., Commo, S., Billoni, N., Mahe, Y.F., Bernard, B.A. (1997). Activation of cytoprotective prostaglandin synthase-1 by minoxidil as a possible explanation for its hair growth-stimulating effect. Journal of Investigative Dermatology. 108(2). 205-209. Available at: https://doi.org/10.1111/1523-1747.ep12334249 |
↑13 | Gupta, A.K., Talukder, M., Venkataraman, M., Bamimore, M.A. (2022). Minoxidil: a comprehensive review. Journal of Dermatological Treatment. 33(4). 1896-1906. Available at: https://doi.org/10.1080/09546634.2021.1945527 |
↑14 | Sattur, S. Talathi, A., Shetty, G., Arsiwala, S., Pereira, R., Dhoot, D. (2023). Comparative Clinical Study Evaluating the Efficacy and Safety of Topical 5% Cetosomal Minoxidil and Topical 5% Alcohol-Based Minoxidil Solutions for the Treatment of Androgenetic Alopecia in Indian Men. Cureus. 15(10). E46568. Available at: https://doi.org/10.7759/cureus.46568 |
↑15, ↑17, ↑20, ↑21, ↑52 | Olsen, E.A., Dunlap, F.E., Funicella, T., Koperski, J.A., Swinehart, J.M., Tschen, E.H., Trancik, R.J. (2002). A randomized clinical trial of 5% topical minoxidil versus 2% topical minoxidil and placebo in the treatment of androgenetic alopecia in men. Journal of the American Academy of Dermatology. 47(3). 377-385. Available at: https://doi.org/10.1067/mjd.2002.124088 |
↑16 | Olsen, E.A., DeLong, E.R., Weiner, M.S. (1987). Long-term follow-up of men with male pattern baldness treated with topical minoxidil. Journal of the American Academy of Dermatology. 16(3 Pt 2). 688-695. Available at: https://doi.org/10.1016/s0190=9622(87)70089-9 |
↑18 | Blume-Peytavi, U., Hillmann, K., Dietz, E., Canfield, D., Bartels, N.G. (2011). A randomized, single-blind trial of 5% minoxidil foam once daily versus 2% minoxidil solution twice daily in the treatment of androgenetic alopecia in women. Journal of the American Academy of Dermatology. 65(6). 1126-1134. Available at: https://doi.org/10.1016/j.jaad.2010.09.724 |
↑19 | Ramos, P.M., Melo, D.F., Radwanski, H., de Almeida, R.F.C., Miot, H.A. (2023). Female-pattern hair loss: therapeutic update. Anais Brasileiros de Dermatologica. 98(4). 506-519. Available at: https://doi.org/10.1016/j.abd.2022.09.006 |
↑22 | Singh, S., Patil, A., Kianfar, N., Waskiel-Burnat, A., Rudnicka, L., Sinclair, R., Goldust, M. (2022). Does topical minoxidil at concentrations higher than 5% provide additional clinical benefit? Clinical and Experimental Dermatology. 47(11). 1951-1955. Available at: https://doi.org/10.1111/ced.15338 |
↑23 | Vasantha, K.L. (2025). Efficiency and Safety of 10% Minoxidil in the Treatment of Alopecia Areata: A Randomised Controlled Trial. Journal of Population Therapeutics and Clinical Pharmacology. 32(4). 724-730. Available at: https://doi.org/10.53555/56ggpq88 |
↑24 | Ghonemy, S., Alarawi, A., Bessar, H. (2021). Efficacy and safety of a new 10% topical minoxidil versus 5% topical minoxidil and placebo in the treatment of male androgenetic alopecia: a trichoscopic evaluation. Journal of Dermatological Treatment. 32(2). 236-241. Available at: https://doi.org/10.1080/09546634.2019.1654070 |
↑25 | Grice, J.E., Ciotti, S., Weiner, N., Lockwood, P., Cross, S.E., Roberts, M.S. (2010). Relative uptake of minoxidil into appendages and stratum corneum and permeation through human skin in vitro. Journal of Pharmaceutical Science. 99(2). 712-718. Available at: https://doi.org/10.1002/jps.21856 |
↑26 | Patel, K., Palmer, A., Nixon, R. (2023). Allergic contact dermatitis from propylene glycol: A case series from Australia. Contact Dermatitis. 89(2). 79-84. Available at: https://doi.org/10.1111/cod.14325 |
↑27 | Nestor, M.S., Ablon, G., Gade, A., Han, H., Fischer, D.L. (2021). Treatment options for androgenetic alopecia: Efficacy, side effects, compliance, financial considerations, and ethics. Journal of Cosmetic Dermatology. 20(12). 3759-3781. Available at: https://doi.org/10.1111/jocd.14537 |
↑28 | Blume-Peytavi, U., Hillmann, K., Dietz, E., Canfield, D., Bartels, N.G. (2011). A randomized, single-blind trial of 5% minoxidil foam once-daily versus 2% minoxidil solution twice daily in the treatment of androgenetic alopecia in women. Journal of the American Academy of Dermatology. 65(6). 1126-1134. Available at: https://doi.org/10.1016/j.jaad.2010.09.724 |
↑29 | Barbareschi, M., Vescovi, V., Starace, M., Piraccini, B.M., Milani, M. (2020). Propylene glycol free 5% minoxidil lotion formulation: cosmetic acceptability, local tolerability, clinical efficacy and in-vitro skin absorption evaluations. Edizioni Minerva Medica. 155(3). 341-345. Available at: https://doi.org/10.23736/S0392-0488.20.06554-2 |
↑30 | Sharma, A., Goren, A., Dhurat, R., Agrawal, S., Sinclair, R., Trueb, R.M., Vano-Galvin, S., Chen, G., Tan, Y., Kovacevic, M., Situm, M., McCoy, J. (2019). Tretinoin enhances minoxidil response in androgenetic alopecia patients by upregulating follicular sulfotransferase enzymes. Dermatologic Therapy. 32(3). 12915. Available at: https://doi.org/10.1111/dth.12915 |
↑31 | Asilian, A., Farmani, A., Saber, M. (2023). Clinical efficacy and safety of low-dose oral minoxidil versus topical solution in the improvement of androgenetic alopecia: A randomized controlled trial. Journal of Cosmetic Dermatology. 23(3). 949-957. Available at: https://doi.org/10.1111/jocd.16086 |
↑32 | Olsen, E.A., Weiner, M.S., Amara, I.A., DeLong, E.R. (1990). Five-year follow-up of men with androgenetic alopecia treated with topical minoxidil. Journal of American Academy of Dermatology. 22(4). 643-646. Available at: https://doi.org/10.1016/0190-9622(90)70089-z |
↑33, ↑53 | Shadi, Z. (2023) Compliance to Topical Minoxidil and Reasons for Discontinuation among Patients with Androgenetic Alopecia. Dermatology and Therapy. 13(5). 1157-1169. Available at: https://doi.org/10.1007/s13555-023-00919-x |
↑34, ↑37 | Van Neste, D. (2020). Placebo-controlled dose-effect studies with topical minoxidil 2% or 5% in male-patterned hair loss treated with oral finasteride employing an analytical and exhaustive study protocol. Skin Research & Technology. 26(4). 542-557. Available at: https://doi.org/10.1111/srt.12827 |
↑35 | [Updated 2023 Feb 24]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK482378/ Accessed: July 2025 |
↑36 | Trueb, R.M., Dias, M.F.R.G., Rezende, H.D. (2021). Comment on Follicular Inflammation and Fibrosis in Pattern Hair Loss. Skin Appendage Disorders. 7(2). 159-160. Available at: https://doi.org/10.1159/000513089 |
↑38 | Ahmed, K.M.A., Kozaa, Y.A., Abuawwad, M.T., Al-Najdawi, A.I.A., Mahmoud, Y.W., Ahmed, A.M., Taha, M.J.J., Fadhli, T., Giannopoulou, A. (2025). Evaluating the efficacy and safety of combined microneedling therapy versus topical Minoxidil in androgenetic alopecia: a systematic review and meta-analysis. Archives of Dermatological Research. 317(1). 528. Available at: https://doi.org/10.1007/s00403-025-04032-1 |
↑39, ↑40, ↑45 | Zhang, Y., Sheng, Y., Zeng, Y., Hu, R., Zhao, J., Wang, W., Yang, Q. (2022). Randomized trial of microneedling combined with 2% minoxidil topical solution for the treatment of female pattern hair loss in a Chinese population. Journal of Cosmetic Dermatology. 21(12). 6985-6991. Available at: https://doi.org/10.1111/jocd.15424 |
↑41 | Sharma, A., Surve, R., Dhurat, R., Sinclair, R., Tan, T., Zou, Y., Ramos, M.P., Wambier, C., Vernier, I., Kovacevic, M., Goren, A. (2020). Microneedling improves minoxidil response in androgenetic alopecia patients by upregulating follicular sulfotransferase enzymes. Journal of Biological Regulators and Homeostatic Agents. 34(2). 659-661. Available at: https://doi.org/10.23812/19-385-L-51 |
↑42 | Sharma, A., Goren, A., Dhurat, R., Agrawal, S., Sinclair, R., Trueb, R.M., Vano-Galvan, S., Chen, G., Tan, Y., Kovacevic, M., Situm, M., McCoy, J. (2019). Tretinoin enhances minoxidil response in androgenetic alopecia patients by upregulating follicular sulfotransferase enzymes. Dermatologic Therapy. 32(3). E12915. Available at: https://doi.org/10.1111/dth.12915 |
↑43 | Dhurat, R., Sukesh, M.S., Avhad, G., Dandale, A., Pal, A., Pund, P. (2013). A Randomized Evaluator Blinded Study of Effect of Microneedling in Androgenetic Alopecia: A Pilot Study. International Journal of Trichology. 5(1). 6-11. Available at: https://doi.org/10.4103/0974-7753.114700 |
↑44 | Kumar, K.M., Inamadar, A.C., Palit, A. (2018). A Randomized Controlled, Single-Observer Blinded Study to Determine the Efficacy of Topical Minoxidil plus Microneedling versus Topical Minoxidil Alone in the Treatment of Androgenetic Alopecia. Journal of Cutaneous and Aesthetic Surgery. 11(4). 211-216. Available at: https://doi/org/10.4103/JCAS.JCAS_130_17 |
↑46 | Ramirez-Marin, H.A., Tosti, A. (2022). Role of Oral Minoxidil in Patterned Hair Loss. Indian Dermatology Online Journal. 13(6). 729-733. Available at: https://doi.org/10.4103/idoj.idoj_246_22 |
↑47 | Gupta, A.K., Talukder, M., Shemer, A., Piraccini, B.M., Tosti, A. (2023). Low-Dose Oral Minoxidil for Alopecia: A Comprehensive Review. Skin Appendage Disorders. 9(6). 423-437. Available at: https://doi.org/10.1159/000531890 |
↑48 | Chemical Book. (no date). Minoxidil Sulphate. ChemBook. Available at: https://www.chemicalbook.com/Price/Minoxidil-sulphate.htm Accessed: July 2025 |
↑49 | Shan, Y., Xu, C., Guo, Y., Wen, L., Zhou, S., Fang, L., Xu, J., Zhen, H. (2025). Liposomes enhance the hair follicle delivery of minoxidil sulfate with improved treatment of androgenetic alopecia. 677. 125642. Available at: https://doi.org/10.1016/j.ijpharm.2025.125642 |
↑50 | Rafi, A.W., Katz, R.M. (2011). Pilot study of 15 patients receiving a new treatment regimen for androgenic alopecia: the effects of atopy on AGA. ISRN Dermatology. 11. 241953. Available at: https://doi.org/10.5402/2011/241953 |
↑51 | Rundegren, J. (2004). Rapid onset of action of minoxidil 5% topical solution in a 4-month German observational study on both patients and physicians. Journal of the American Academy of Dermatology. 50(3). 91. Available at https://doi.org/10.1016/j.jaad.2003.10.290 |
↑54 | Jadeed, H.B., Almudimeegh, A.M., Alomran, S.A., Alshathry, A.H. (2021). A Case of Contact Allergic Dermatitis to Topical Minoxidil. Cureus. 13(1). E12510. Available at: https://doi.org/10.7759/cureus.12510 |
↑55 | Chellini, P.R., Pirmez, R., Raso, P., Sodre, C.T. (2015). Generalized hypertrichosis induced by topical minoxidil in an adult woman. International Journal of Trichology. 7(4). 182-183. Available at: https://doi.org/10.4103/0974-7753.171587 |
↑56 | DeClementi, C., Bailey, K.L., Goldstein, S.C., Orser, M.S. (2004). Suspected toxicosis after topical administration of minoxidil in 2 cats. Veterinary Emergency & Critical Care. 14(4). 287-292. Available at: https://doi.org/10.1111/j.1476-4431.2004.04014.x |
↑57 | Leenen, F.H., Smith, D.L., Unger, W.P. (1988). Topical minoxidil: cardiac effects in bald man. British Journal of Clinical Pharmacology. 26(4). 481-485. Available at: https://doi.org/10.1111/j.1365-2125.1988.tb03410.x |
↑58, ↑59 | Price, V.H., Menefee, E., Strauss, P.C. (1999). Changes in hair weight and hair count in men with androgenetic alopecia, after application of 5% and 2% topical minoxidil, placebo, or no treatment. Journal of the American Academy of Dermatology. 41(5). 717-721. https://doi.org/10.1016/S0190-9622(99)70006-X |
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Learn MoreDr. Sarah King is a researcher & writer who holds a BSc in Medical Biology, an MSc in Forensic Biology, and a Ph.D. in Molecular and Cellular Biology. While at university, Dr. King’s research focused on cellular aging and senescence through NAD-dependent signaling – along with research into prostaglandins and their role in hair loss. She is a co-author on several upcoming manuscripts with the Perfect Hair Health team.
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