What is an estradiol patch?
An adhesive worn on the skin that releases estradiol into the bloodstream without passing through the liver first, changed weekly or twice weekly by product. 5 of the 5 women's platforms we track dispense one, published from $58 a month. The route matters: transdermal estrogen carried lower venous thromboembolism risk than oral in the BMJ 2019 data.
Supply is the other variable right now. The patch tracker carries live per-provider availability against the ASHP shortage listing. The route comparison is Vinogradova et al, HRT and risk of venous thromboembolism, BMJ 2019.
What is vaginal estrogen and what does it cost?
Wisp publishes the cheapest at $20, and 5 of the 5 women's platforms we track dispense a vaginal form. Each bills it on a different unit, so the verbatim strings are below rather than a single invented per-month figure. It is dosed far below systemic therapy and treats local symptoms.
- WispEstradiol vaginal cream, from $20 [Verified July 2026]
- Hone HealthEstradiol vaginal cream (Estrace, $40/mo medication estimate; Premium membership and initial testing extra) [Verified September 9, 2026]
- Hone HealthEstradiol vaginal inserts (Vagifem, $65/mo medication estimate; Premium membership and initial testing extra) [Verified September 9, 2026]
- Gala HealthVaginal estradiol — a local treatment option in the advertised $69/month HRT plan, subject to clinician selection and confirmation of the exact prescription and checkout charge [Verified September 9, 2026]
- WinonaVaginal estrogen cream ($89 per 28 days)
Vaginal estrogen is generally considered separately from systemic HRT in the risk discussion, and ACOG's menopause guidance calls the vaginal ring, tablet and cream "local" estrogen therapy, prescribed for vaginal symptoms. Every estradiol form compared.
Is testosterone approved for menopausal women?
No. In FDA's own words in a notice published 2026-08-18: "Unlike estrogen-containing products, there are no FDA approved indications for testosterone therapy for menopausal women." It is prescribed to women anyway, and FDA says so in the same notice: "Nevertheless, the off-label use of testosterone in women nearing or after menopause has increased over the past decade." That makes every prescription of testosterone to a menopausal woman in the United States an off-label one, whatever the clinic calls it. Elsewhere the picture differs: "Testosterone is currently approved for hypoactive sexual desire disorder (HSDD) in women in Australia, New Zealand, the UK, and South Africa." On the evidence, FDA is direct that it is thin. "Beyond HSDD, there are limited data on the treatment effect of testosterone for other clinical uses. While short-term safety data exist for physiologic doses, long-term safety data beyond 24 months are limited, particularly regarding cardiovascular and breast cancer risks." FDA is holding a public workshop on September 17, 2026, 9:00 a.m. to 4:30 p.m. Eastern Time, and taking public comments on docket FDA-2026-N-5479 until October 19, 2026, 11:59 p.m. Eastern Time. 27 comments had already been filed as of 2026-08-26.
None of our women's-wing platforms is scored on testosterone, because there is no approved indication to score them against. If a clinic offers you testosterone for menopause symptoms, the questions worth asking are which symptom it is meant to treat, what dose and what form, whether it is a compounded product, and what the monitoring plan is. FDA's own summary of what is known is worth reading before that conversation: “The role of declining ovarian testosterone levels in menopausal women and its relationship to medical conditions, such as frailty, depressive symptoms, sleep, sexual function, cognition, and musculoskeletal health, are not well understood.”
The dates, if you want a say
- September 10, 2026, 11:59 p.m. Eastern Time is the cutoff to register to attend in person. Those planning to attend virtually may register up until the date of the meeting. Registration is free and based on space availability, with priority given to early registrants.
- September 17, 2026, the workshop itself, 9:00 a.m. to 4:30 p.m. Eastern Time. Hybrid: webcast, plus an in-person option at the FDA White Oak Campus, Great Room, Bldg. 31, Silver Spring, MD.
- October 19, 2026, 11:59 p.m. Eastern Time is when public comments close on docket FDA-2026-N-5479. The notice warns: “Please note that late, untimely filed comments will not be considered.” Anyone may file, patients included.
Source: Testosterone Use in Menopausal Women; Public Workshop; Request for Comments, 91 FR 53417, Notice of public workshop. Read 2026-08-26. We have no commercial interest in this question and no partner selling testosterone to women.
What are HRT pellets?
Hormone implants placed under the skin, and none of the 6 platforms on our roster offers them, so every pellet price you find belongs to a clinic we have not scored. Once a pellet is in, the dose cannot be adjusted, and stopping means waiting it out. Compounded pellets are not FDA-approved.
What the word bioidentical does and does not mean: bioidentical HRT. FDA on human drug compounding.