Men: Is Topical Minoxidil Safe While Trying to Conceive?
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Men: Is Topical Minoxidil Safe While Trying to Conceive?

First Published Nov 12 2025
Last Updated Nov 12 2025
Pharmaceutical
Researched & Written By:
Michael Williams, PhD
Reviewed By:
Rob English, Medical Editor
Men: Is Topical Minoxidil Safe While Trying to Conceive?

Article Summary

Many men use topical minoxidil to combat hair loss, but is it safe to continue while trying to conceive? Curious how the science stacks up and what experts actually recommend? Explore our evidence-based review to learn the facts about topical minoxidil and male fertility.

Full Article

Topical minoxidil is one of the most widely used treatments for androgenic alopecia (AGA) in both men and women. While its efficacy and safety as a hair growth stimulant are well established, some men express concern about whether continuing hair loss treatments is safe when trying to conceive. These concerns often stem from known reproductive warnings associated with other medications, particularly finasteride, which directly influences hormonal pathways. Minoxidil, however, works through entirely different mechanisms, enhancing blood flow, prolonging the hair growth phase, and stimulating follicular activity.

This article examines the available scientific evidence to determine whether topical minoxidil has any measurable effect on male fertility. By reviewing preclinical studies, clinical trials, and pharmacologic data, we aim to clarify whether there is any credible link between minoxidil use and changes in reproductive hormones, sperm quality, or conception outcomes.

How Does Minoxidil Work?

Topical minoxidil stimulates hair growth primarily by increasing blood flow and nutrient delivery to hair follicles. Once applied to the scalp, it’s converted by the enzyme sulfotransferase (SULT1A1) into its active metabolite, minoxidil sulfate, which promotes follicular cell proliferation and prolongs the anagen (growth) phase of the hair cycle. It also upregulates vascular endothelial growth factor (VEGF) and activates potassium channels, both of which create a more favorable microenvironment for hair growth.[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

Many people choose topical minoxidil over oral formulations because it offers similar local benefits with minimal systemic absorption. This greatly reduces the risk of side effects such as water retention, hypertrichosis (excess body hair), or cardiovascular symptoms sometimes seen with oral minoxidil. As an over-the-counter option with a well-established safety profile, topical minoxidil remains the most accessible first-line treatment for AGA.

Male Fertility: What Matters When Trying to Conceive?

Male fertility is defined as the ability to produce viable sperm capable of fertilizing an egg, and is impacted by a wide range of factors. These include hormonal regulation of sperm production, urogenital abnormalities, genetic factors, and environmental factors such as diet, obesity, and cigarette smoking. Semen quality is the best single snapshot of male reproductive potential. Sperm count influences the statistical odds that enough sperm reach the egg; sperm motility determines whether sperm can traverse cervical mucus, the uterus, and the fallopian tube; and morphology reflects the proportion of intact sperm likely to bind and penetrate the egg. These parameters work together, so clinicians interpret them as a profile rather than in isolation.[2]StatPearls; Male Infertility. Available at: https://www.ncbi.nlm.nih.gov/books/NBK562258/ (Accessed: October 2025)

Importantly, medications or drugs can influence many aspects of sperm production and function. Certain prescription drugs, such as anabolic steroids, testosterone supplements, finasteride, spironolactone, and some antidepressants or antihypertensives, can suppress the hormonal pathways that regulate spermatogenesis, reducing sperm count or motility. Others may interfere with sperm maturation, DNA integrity, or seminal fluid composition, leading to poorer fertilization potential. Even topical or seemingly localized medications can, in rare cases, exert mild systemic effects that alter reproductive hormones or oxidative balance.[3]Semet, M., Paci, M., Saïas‐Magnan, J., Metzler‐Guillemain, C., Boissier, R., Lejeune, H., & Perrin, J. (2017). The impact of drugs on male fertility: a review. Andrology. 5(4). 640-663. … Continue reading 

For this reason, men actively trying to conceive are often advised to review all current medications and supplements with a clinician to assess potential reproductive impacts and, if necessary, explore safer alternatives or temporary adjustments.

Systemic Absorption of Topical Minoxidil: How Much Gets In?

Topical minoxidil is designed to act locally on the scalp, with only a small fraction of the drug entering the bloodstream. Studies estimate that around 1-2% of applied minoxidil is systemically absorbed through intact skin, though this can vary depending on factors such as scalp condition, formulation type, and frequency of use. 

For instance, alcohol-based liquid solutions may enhance penetration slightly more than foam preparations, while damaged or inflamed skin can increase absorption. The scalp’s stratum corneum serves as the main barrier, limiting systemic exposure and ensuring that most of the drug remains localized to hair follicles.[4]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

In contrast, oral minoxidil is fully absorbed into systemic circulation and metabolized in the liver, resulting in significantly higher plasma concentrations of active minoxidil sulfate. This explains why oral therapy, though often more potent, also carries a greater risk of systemic side effects, including edema, tachycardia, and generalized hypertrichosis.[5]Randolph, M., & Tosti, A. (2021). Oral minoxidil treatment for hair loss: a review of efficacy and safety. Journal of the American Academy of Dermatology. 84(3). 737-746. Available at: … Continue reading Topical use, by comparison, delivers similar follicular benefits with a much lower risk profile, making it the preferred option for those seeking targeted hair regrowth.

Does Topical Minoxidil Affect Male Fertility?

Topical minoxidil might raise concerns for men trying to conceive, as its activity and impact are related to hormonally sensitive pathways. To explore this question properly, we can look at the evidence from laboratory models, human studies, and systematic analyses to understand any potential risks. 

Preclinical Evidence

Other hair loss treatments, such as finasteride, act on hormonal pathways to alter the activity of androgens like testosterone. They may therefore pose a risk to male fertility. As such, it’s important to establish the impact of minoxidil on hormonal factors such as androgen response.

Animal models, particularly those involving rodents and primates, have primarily examined hair cycle dynamics rather than reproductive parameters. These studies consistently show that minoxidil promotes the transition of hair follicles from the telogen (resting) to anagen (growth) phase, enlarges follicular structures, and increases local blood flow. 

One study using golden Syrian hamsters showed that 5% topical minoxidil did not prevent the androgen-dependent growth of pigmented spots, suggesting that minoxidil does not have any effect on androgen response.[6]Nuck, B. A., Fogelson, S. L., & Lucky, A. W. (1987). Topical minoxidil does not act as an antiandrogen in the flank organ of the golden Syrian hamster. Archives of Dermatology. 123(1). 59-61. … Continue reading 

In contrast, a more recent, small-scale study using rats investigated the impact of topical minoxidil on sperm health. They found that the experimental group, receiving 10% minoxidil, had a 12-13% decline in testicular weight compared to the controls, as well as increases in markers related to oxidative stress within the testicles.[7]Turkina, V., Chemodurova, N., Hrushka, O., & Pryzyhlei, H. (2020). Topical effect of minoxidil-containing lotion on morphofunctional indicators of male rats’ reproductive system. … Continue reading Unfortunately, the authors do not specify the volume of 10% minoxidil used, making it impossible to make a concrete comparison to normal dosing in humans. This makes the translatability of these toxicology studies more challenging.

Research using cell-based models, including human hair dermal papilla cells, suggests that minoxidil can directly interact with and weaken androgen receptor signaling. However, this study used higher concentrations of minoxidil than would be used in hair loss treatment, and for practical purposes, topical minoxidil remains classified as a non-hormonal treatment.[8]Hsu, C. L., Liu, J. S., Lin, A. C., Yang, C. H., Chung, W. H., & Wu, W. G. (2014). Minoxidil may suppress androgen receptor‐related functions. Oncotarget. 5(8). 2187-2197. Available at: … Continue reading

Figure 1: In vitro studies show a potential effect of minoxidil on androgen receptor activity. Adapted from:[9]Hsu, C. L., Liu, J. S., Lin, A. C., Yang, C. H., Chung, W. H., & Wu, W. G. (2014). Minoxidil may suppress androgen receptor‐related functions. Oncotarget. 5(8). 2187-2197. Available at: … Continue reading Image used in accordance with the Creative Commons Attribution Licence.

Clinical Evidence

While preclinical studies can provide insights into minoxidil activity, evidence for its effect and potential risks should be derived primarily from studies in humans. In clinical settings, topical minoxidil has been studied extensively for AGA, with trials ranging from short-term safety assessments to large randomized controlled trials. Across numerous studies, using 2%, 3%, 5%, and even 10% topical concentrations, the most commonly reported adverse events have been mild scalp irritation, contact dermatitis, or unwanted hair growth on non-target areas.[10]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 … Continue reading,[11]Hasanzadeh, H., Nasrollahi, S. A., Halavati, N., Saberi, M., & Firooz, A. (2016). Efficacy and safety of 5% minoxidil topical foam in male pattern hair loss treatment and patient satisfaction. … Continue reading,[12]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 … Continue reading 

One randomized trial of 149 subjects reported two cases of impotence during the study, which disappeared following discontinuation of minoxidil treatment.[13]Rietschel, R. L., & Duncan, S. H. (1987). Safety and efficacy of topical minoxidil in the management of androgenetic alopecia. Journal of the American Academy of Dermatology. 16(3). 677-685. … Continue reading This was the only case of sexual side effects we could find, and it seems to represent a rare complaint. Notably, however, none of these trials have reported reproductive or hormonal disturbances. 

One randomized, controlled study that compared the impact of topical minoxidil alone to a solution containing 0.25% finasteride and 3% minoxidil explicitly monitored sexual side effects. The trial assessed levels of dihydrotestosterone (DHT), a marker for androgen suppression that may be relevant to male fertility. The report found a modest decrease in DHT only in the group who also applied finasteride, suggesting that minoxidil did not impact androgen activity.[14]Suchonwanit, P., Srisuwanwattana, P., Chalermroj, N., & Khunkhet, S. (2018). A randomized, double-blind controlled study of the efficacy and safety of topical solution of 0.25% finasteride … Continue reading

The largest comparative analysis to date, using the FDA Adverse Event Reporting System (FAERS) data, reinforces these findings. Over ten years of reporting revealed that finasteride was associated with markedly higher rates of erectile dysfunction, decreased libido, and ejaculatory disorders. In contrast, minoxidil, both topical and oral, was not associated with reproductive toxicity in either men or women. Dermatologic reactions such as irritation or dermatitis were the only consistent signals. This post-marketing evidence, covering thousands of patients, supports the conclusion that minoxidil does not interfere with male sexual function or fertility.[15]Wu, M., Yu, Q., & Li, Q. (2016). Differences in reproductive toxicology between alopecia drugs: an analysis on adverse events among female and male cases. Oncotarget. 7(50). 82074-82084. … Continue reading

It is worth noting that most clinical studies do not measure semen parameters, testosterone, or dihydrotestosterone (DHT) levels in participants, so while there is no evidence of harm, data on direct fertility endpoints remain limited. However, trials that have assessed hormonal changes indirectly, such as topical finasteride-minoxidil combinations, report only minimal and clinically insignificant reductions in DHT, well within physiologic ranges and unlikely to impact spermatogenesis. Collectively, this body of evidence supports that topical minoxidil, when used at therapeutic concentrations, exerts its effects locally on hair follicles without meaningful systemic hormonal consequences.

Comparison to Other Hair Loss Treatments

Compared with other medical treatments for hair loss, topical minoxidil has a distinctly favorable reproductive safety profile. Finasteride and dutasteride, both 5-α-reductase inhibitors, work by suppressing the conversion of testosterone to DHT, a potent androgen involved in follicular miniaturization. While effective, this mechanism directly influences sex hormone pathways and has been associated in some users with reduced libido, erectile dysfunction, decreased semen volume, and abnormal sperm morphology.[16]Gupta, A. K., Venkataraman, M., Talukder, M., & Bamimore, M. A. (2022). Finasteride for hair loss: a review. Journal of Dermatological Treatment. 33(4). 1938-1946. Available at: … Continue reading,[17]Estill, M. C., Ford, A., Omeira, R., & Rodman, M. (2023). Finasteride and dutasteride for the treatment of male androgenetic alopecia: a review of efficacy and reproductive adverse effects. … Continue reading 

Topical minoxidil, in contrast, exerts no effect on androgen synthesis or receptor binding, acts locally, and is absorbed systemically at rates of roughly 1-2%. Clinical and pharmacologic studies have not detected significant changes in serum hormones, testicular function, or sperm parameters associated with its use. For men attempting to conceive, topical minoxidil is therefore considered the safer option when pharmacologic hair restoration is desired.

Summary Consensus

No systematic reviews or meta-analyses have found an association between topical minoxidil and male reproductive dysfunction. Across clinical trials and pharmacovigilance datasets (such as FAERS), the consensus remains that topical minoxidil poses minimal to no risk to male fertility. Its non-hormonal mechanism stands in contrast to antiandrogenic drugs like finasteride or dutasteride, which are known to suppress DHT levels and can cause sexual side effects in some users. 

The absence of evidence of reproductive toxicity for topical minoxidil is notable given its widespread use over several decades. Still, it is important to acknowledge that the absence of evidence is not definitive proof of absence, and few studies have directly measured sperm quality or fertility outcomes, leaving a modest evidence gap for future research.

Counseling and Clinical Recommendations

Professional society guidelines, including those from the American Academy of Dermatology (AAD), European Academy of Dermatology and Venereology (EADV), and National Institute for Health and Care Excellence (NICE), all recognize topical minoxidil as a first-line treatment for AGA. None include warnings about male fertility or recommend discontinuing treatment when trying to conceive. Recommendations against use in pregnancy and breastfeeding are directed exclusively at women due to potential fetal exposure, not paternal risk.[18]Olsen, E. A., Sinclair, R., Hordinsky, M., Mesinkovska, N. A., Sadick, N., Shapiro, J., & Bergfeld, W. (2025). Summation and recommendations for the safe and effective use of topical and oral … Continue reading

In clinical practice, dermatologists generally reassure male patients that topical minoxidil can be safely continued when planning conception. They may, however, emphasize good application hygiene, using the prescribed dose, applying only to the scalp, washing hands afterward, and allowing the product to dry fully before physical contact to prevent unintended transfer to partners or infants. Because systemic absorption is minimal, these precautions are primarily to avoid topical irritation rather than systemic effects. 

Myths and Misconceptions About Topical Minoxidil and Fertility

Given the links between minoxidil activity and hormonally sensitive pathways related to hair loss, some men may have concerns about using the medication when trying to conceive. Let’s look at some of the potential misconceptions about topical minoxidil and fertility.

Topical minoxidil causes infertility

There is some limited evidence from animal studies suggesting that topical minoxidil may affect sperm quality.[19]Turkina, V., Chemodurova, N., Hrushka, O., & Pryzyhlei, H. (2020). Topical effect of minoxidil-containing lotion on morphofunctional indicators of male rats’ reproductive system. … Continue reading However, there is no evidence that topical minoxidil reduces sperm count, motility, or morphology. Clinical trials of 3%, 5%, and 10% minoxidil report vanishingly few reproductive or hormonal side effects. The drug acts locally on the scalp, with systemic absorption of only about 1–2%, far below levels that could influence reproductive physiology. Neither animal studies nor human trials have identified any fertility-related toxicity associated with topical minoxidil use.

Topical minoxidil alters male hormone levels

Studies suggest that minoxidil does not interfere with androgen production, metabolism, or receptor binding at doses relevant for hair loss. It promotes hair growth through vascular and cellular mechanisms, such as increasing VEGF expression and opening potassium channels, not by modifying testosterone or dihydrotestosterone (DHT) pathways. 

However, some research using cell-based models has suggested that minoxidil might impact androgen receptor activity at high concentrations.[20]Hsu, C. L., Liu, J. S., Lin, A. C., Yang, C. H., Chung, W. H., & Wu, W. G. (2014). Minoxidil may suppress androgen receptor‐related functions. Oncotarget. 5(8). 2187-2197. Available at: … Continue reading

Topical minoxidil causes erectile dysfunction

Sexual side effects are very rarely reported in any major clinical trials or pharmacovigilance data concerning topical minoxidil, with only two cases of impotence associated with topical minoxidil reported in the literature. Erectile dysfunction, decreased libido, and ejaculatory changes are associated with oral 5-α-reductase inhibitors (such as finasteride), not with topical minoxidil.[21]Wu, M., Yu, Q., & Li, Q. (2016). Differences in reproductive toxicology between alopecia drugs: an analysis on adverse events among female and male cases. Oncotarget. 7(50). 82074-82084. … Continue reading

Fertility risks are the same for all hair loss drugs

Different hair loss treatments have fundamentally different mechanisms. Finasteride and dutasteride lower DHT and can influence sexual function and semen parameters in some users.[22]Estill, M. C., Ford, A., Omeira, R., & Rodman, M. (2023). Finasteride and dutasteride for the treatment of male androgenetic alopecia: a review of efficacy and reproductive adverse effects. … Continue reading Minoxidil, on the other hand, does not interact with the androgen pathway and has no known reproductive risks. Therefore, the fertility profile of topical minoxidil is significantly safer than that of antiandrogenic agents.

Final Thoughts

Topical minoxidil remains one of the safest and most accessible treatments for male pattern hair loss, with decades of research supporting its efficacy and tolerability. Unlike hormone-modulating therapies such as finasteride, minoxidil works through non-androgenic pathways and shows no evidence of affecting male fertility, hormone levels, or sexual function. While future studies could further clarify long-term reproductive outcomes, the current consensus is clear: topical minoxidil is a fertility-neutral, first-line option for men looking to manage hair loss safely.

References

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
2 StatPearls; Male Infertility. Available at: https://www.ncbi.nlm.nih.gov/books/NBK562258/ (Accessed: October 2025)
3 Semet, M., Paci, M., Saïas‐Magnan, J., Metzler‐Guillemain, C., Boissier, R., Lejeune, H., & Perrin, J. (2017). The impact of drugs on male fertility: a review. Andrology. 5(4). 640-663. Available at: https://doi.org/10.1111/andr.12366
4 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
5 Randolph, M., & Tosti, A. (2021). Oral minoxidil treatment for hair loss: a review of efficacy and safety. Journal of the American Academy of Dermatology. 84(3). 737-746. Available at: https://doi.org/10.1016/j.jaad.2020.06.1009
6 Nuck, B. A., Fogelson, S. L., & Lucky, A. W. (1987). Topical minoxidil does not act as an antiandrogen in the flank organ of the golden Syrian hamster. Archives of Dermatology. 123(1). 59-61. Available at: https://doi.org/10.1001/archderm.1987.01660250065019
7, 19 Turkina, V., Chemodurova, N., Hrushka, O., & Pryzyhlei, H. (2020). Topical effect of minoxidil-containing lotion on morphofunctional indicators of male rats’ reproductive system. Український журнал сучасних проблем токсикології. (2). 27-31. Available at: https://protox.medved.kiev.ua/index.php/en/issues/2020/2/item/633-topical-effect-of-minoxidil-containing-lotion-on-morphofunctional-indicators-of-male-rats-reproductive-system
8 Hsu, C. L., Liu, J. S., Lin, A. C., Yang, C. H., Chung, W. H., & Wu, W. G. (2014). Minoxidil may suppress androgen receptor‐related functions. Oncotarget. 5(8). 2187-2197. Available at: /https://doi.org/10.18632/oncotarget.1886
9, 20 Hsu, C. L., Liu, J. S., Lin, A. C., Yang, C. H., Chung, W. H., & Wu, W. G. (2014). Minoxidil may suppress androgen receptor‐related functions. Oncotarget. 5(8). 2187-2197. Available at: /https://doi.org/10.18632/oncotarget.1886
10 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
11 Hasanzadeh, H., Nasrollahi, S. A., Halavati, N., Saberi, M., & Firooz, A. (2016). Efficacy and safety of 5% minoxidil topical foam in male pattern hair loss treatment and patient satisfaction. Acta Dermatovenerol Alp Pannonica Adriat. 25(3). 41-44. Available at: https://doi.org/10.15570/actaapa.2016.12
12 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
13 Rietschel, R. L., & Duncan, S. H. (1987). Safety and efficacy of topical minoxidil in the management of androgenetic alopecia. Journal of the American Academy of Dermatology. 16(3). 677-685. Available at: https://doi.org/10.1016/S0190-9622(87)70087-5
14 Suchonwanit, P., Srisuwanwattana, P., Chalermroj, N., & Khunkhet, S. (2018). A randomized, double-blind controlled study of the efficacy and safety of topical solution of 0.25% finasteride admixed with 3% minoxidil vs. 3% minoxidil solution in the treatment of male androgenetic alopecia. Journal of the European Academy of Dermatology and Venereology. 32(12). 2257-2263. Available at: https://doi.org/10.1111/jdv.15171
15, 21 Wu, M., Yu, Q., & Li, Q. (2016). Differences in reproductive toxicology between alopecia drugs: an analysis on adverse events among female and male cases. Oncotarget. 7(50). 82074-82084. Available at: https://doi.org/10.18632/oncotarget.12617
16 Gupta, A. K., Venkataraman, M., Talukder, M., & Bamimore, M. A. (2022). Finasteride for hair loss: a review. Journal of Dermatological Treatment. 33(4). 1938-1946. Available at: https://doi.org/10.1080/09546634.2021.1959506
17 Estill, M. C., Ford, A., Omeira, R., & Rodman, M. (2023). Finasteride and dutasteride for the treatment of male androgenetic alopecia: a review of efficacy and reproductive adverse effects. Georgetown Medical Review. 7(1). Available at: https://doi.org/10.52504/001c.88531
18 Olsen, E. A., Sinclair, R., Hordinsky, M., Mesinkovska, N. A., Sadick, N., Shapiro, J., & Bergfeld, W. (2025). Summation and recommendations for the safe and effective use of topical and oral minoxidil. Journal of the American Academy of Dermatology. 93(2). 457-465. Available at: https://doi.org/10.1016/j.jaad.2025.04.016
22 Estill, M. C., Ford, A., Omeira, R., & Rodman, M. (2023). Finasteride and dutasteride for the treatment of male androgenetic alopecia: a review of efficacy and reproductive adverse effects. Georgetown Medical Review. 7(1). Available at: https://doi.org/10.52504/001c.88531
Michael Williams, PhD

Michael Williams, PhD

Michael is a researcher and writer who holds a BSc in Bioscience, an MSc in Regenerative Medicine, and a PhD in Translational Biomedicine. He undertook his PhD research at Houston Methodist Research Institute, Texas, focusing on cell signaling in the ovarian cancer tumor microenvironment. He conducted postdoctoral research at Barts Cancer Institute in London, exploring cellular metabolism in acute myeloid leukemia. He has published work in a range of fields, including oncology, nanomedicine, and cell-based therapeutics.

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