WOMEN'S HRT
Estradiol Gel
Prescription estradiol gel delivers systemic estrogen through the skin in an adjustable daily format.
From $79/mo
Compounded cream
Biest 80:20
A compounded estriol-forward 80:20 blend that makes its formulation logic visible instead of hiding it in pharmacy fine print.
Your treatment plan
$89/month
Our team can help with treatment options, pricing and next steps.
- Licensed clinicians
- Compounded by a licensed 503A pharmacy
- No clinic visit
Questions before you start?
Compare this treatmentWhat will I pay?
Our team can help with treatment options, pricing and next steps. Contact our team for pharmacy and fulfillment details for this treatment.
View full plan detailsWhat should I know about this treatment?
A compounded estriol-forward 80:20 blend that makes its formulation logic visible instead of hiding it in pharmacy fine print.
Read the evidence and its limitationsWhat should I review before starting?
Boxed warning
The approved labeling for estradiol is therefore the best available guide to what this class does, and it carries a boxed warning that estrogen without a progestogen increases the risk of endometrial cancer in a woman who still has a uterus, so unopposed estrogen is not an appropriate plan in that situation and progesterone belongs in the conversation.
A licensed clinician reviews your health history and medications and determines whether treatment is appropriate for you.
Read the full Important Safety InformationWhat happens next?
Our team can help with treatment options, pricing and next steps. Contact our team for pharmacy and fulfillment details for this treatment.
Ask about this treatmentWhat It Is
The ratio is a prescribing decision, not a preference.
Biest combines two bioidentical estrogens, estriol and estradiol, in one topical preparation. Estradiol is the body’s most potent estrogen. Estriol is weaker. In an 80:20 preparation the formula is weighted four to one toward estriol, so a smaller share of the total estrogen is the potent one. It is prepared as a measured cream to the prescription your clinician writes for you.
That ratio is the clinical distinction from the 50:50 blend.
Two clinicians looking at two patients can reach different conclusions about how much of the total should be estradiol. Compounding is what lets that judgment be written into the prescription rather than approximated with the nearest commercial product. The ratio is chosen by your provider from your clinical picture. It is not a strength you select, and a different ratio is not an upgrade.
The 80:20 preparation gives your clinician a defined estriol-forward option when your clinical picture supports an individualized ratio, strength, or cream base.
An 80:20 formulation contains four parts estriol to one part estradiol. Your clinician determines whether that balance belongs in your individual prescription.
Read the evidenceWho It's For
For the patient whose clinician has a reason for this ratio.
01
The Ratio Was a Considered Choice
Your clinician has a specific reason to weight the formula toward estriol rather than split it evenly. That reasoning belongs in your notes, and you should be able to hear it in plain language.
02
Standard Options Did Not Fit Cleanly
You have tried or considered commercial estradiol formats and, with your clinician, have a documented reason to look at a different strength, combination, or base.
03
You Want the Variables in Clinical Hands
Ratio, strength, base, dose, and follow-up create more room to tailor. That flexibility is valuable only when someone qualified is responsible for using it well.
Compounded Biest 80:20 is not an FDA-approved drug product, and compounded bioidentical hormones have not been shown to be safer or more effective than FDA-approved hormone therapy. The estriol to estradiol ratio is determined by your provider and is not selectable at checkout. A licensed provider determines whether a compounded preparation fits your case, or whether an approved therapy serves you better.
This might not be the right fit if:
- History of breast cancer or another estrogen-dependent malignancy
- Unexplained vaginal bleeding
- History of blood clots, stroke, or heart attack
- Active liver disease
- Pregnancy or planned pregnancy
Your intake screens for all contraindications. Every candidate is evaluated by a licensed clinician before any prescription is issued. No prescription is issued without clearance.
Your Plan
Biest 80:20, prescribed with care.
Compounded by a licensed 503A pharmacy. Prescribed by a licensed provider after clinical review.
- Format
- Compounded cream
- Strength
- 0.5% (5 mg/g), 80:20 estriol to estradiol
- Total plan quantity
- 30 g
- Billed amount
- $89 monthly
- Fees
- Included in the plan price
Strength describes the preparation. Total plan quantity is the amount included in that plan, not your dose or dosing schedule. Follow the directions on your prescription.
Biest 80:20
Compounded cream
$89
Billed monthly. All fees included.
- Estriol and estradiol combined 80:20 in a topical cream
- Compounded by a licensed 503A pharmacy to your clinician’s specification
- Applied as directed by your clinician
- Paired with progesterone when you have a uterus, per standard of care
- Reviewed and adjusted through your ongoing provider relationship
Our team can help with treatment options, pricing and next steps.
Ask about this treatmentPrescription issued subject to provider judgment. Results vary. Not a guarantee of outcomes.
Have a question about this plan?
Clinical questions
Message your provider about dosing, side effects, your response or changes in your health.
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The people behind your care
Guidance from the first question onward.
Independent clinical care
Licensed clinicians affiliated with Arora Health & Aesthetics, LLC review your health history, medications and goals, then discuss whether Biest 80:20 or another approach fits your needs.
Medical information on this page reviewed by Dr. Dylan Russell, MD, Chief Health Officer on . Your prescribing clinician provides your individual care.
Verify Dr. Russell's medical licensePharmacy quality that matters
Prepared to your prescription by a licensed compounding pharmacy. Our partners have verified quality programs covering identity, potency, independent testing and batch documentation.
Compounded preparations are not FDA-approved. Pharmacy quality controls and your clinician's evaluation of treatment evidence each have a role in your care.
Pharmacy & fulfillment
Contact our team for pharmacy and fulfillment details for this treatment.
A direct line for follow-up
Message your provider through the patient portal about dosing, side effects, your response or changes in your health. Contact AnthologyRX support for billing, shipment or portal-access help.
The Evidence
What the research shows
The National Academies found insufficient evidence for compounded bioidentical hormone therapy.
2020
consensus report convened at the FDA’s request
The detail
The question has been reviewed at the highest level available. At the FDA’s request, the National Academies of Sciences, Engineering, and Medicine convened a committee that reviewed the uses of compounded bioidentical hormone therapy and the evidence behind its marketing claims, with a prioritized focus that included estradiol and estriol. Its 2020 consensus report concluded, in its own words, that given the paucity of data on the safety and effectiveness of compounded bioidentical hormone therapy there is insufficient evidence to support its overall clinical utility as a treatment for menopause symptoms.1
Prescribers should restrict compounding to a documented allergy or documented need for a different dosage form.
Recommendation 1
patient preference alone should not determine use
The detail
That report also made a specific prescribing recommendation. Recommendation 1 is that prescribers restrict the use of compounded bioidentical hormone therapy to a documented allergy to an active pharmaceutical ingredient or excipient of an FDA-approved drug product, or a documented requirement for a different dosage form, and that patient preference alone should not determine use. That recommendation is why an individualized preparation has to be justified rather than requested.1
The one positive efficacy finding was for vaginal androgen, not a compounded estrogen cream.
29 trials · 1,808 women
compounded preparations compared with placebo or FDA-approved products
The detail
The most recent systematic review and meta-analysis of the field pooled 29 randomized controlled trials reported in 40 articles, covering 1,808 perimenopausal and postmenopausal women, comparing compounded preparations with placebo or with FDA-approved products. It found no adverse change in lipid profile or glucose metabolism with compounded androgen, no change in endometrial thickness and no serious adverse events across the included trials. Its one positive efficacy finding was for compounded vaginal androgen in vaginal atrophy symptoms, standardized mean difference minus 0.66, 95 percent confidence interval minus 1.28 to minus 0.04, not for a compounded estrogen cream.2
On estrogen alone, hyperplasia was common; every estrogen plus progestin regimen matched placebo.
27.7 vs 0.8 percent
simple hyperplasia on estrogen alone versus placebo
The detail
What unopposed estrogen does to the uterine lining is established, and it is why progesterone is in this conversation. In the Postmenopausal Estrogen/Progestin Interventions trial, a 3-year randomized, double-masked, placebo-controlled trial in 596 postmenopausal women aged 45 to 64, women on estrogen alone developed simple hyperplasia in 27.7 percent of cases, complex hyperplasia in 22.7 percent and atypical hyperplasia in 11.8 percent, against 0.8 percent, 0.8 percent and 0 percent on placebo, p less than 0.001, while all three estrogen plus progestin regimens matched placebo, p equals 0.16.3
What it does not show
No randomized trial has tested this 80:20 estriol and estradiol cream.
80:20
estriol to estradiol cream, untested in any controlled trial
The detail
No randomized trial has tested this preparation as sold. There is no controlled trial of an 80:20 estriol and estradiol compounded cream for menopausal symptoms in the published literature, so there is no efficacy figure, no dose-response curve and no safety database that belongs to this specific formulation. The National Academies committee that reviewed the whole field reached the same conclusion about the category: insufficient evidence to support routine clinical use.1
Estradiol’s randomized results belong to approved products, not to a compounded cream.
The detail
The estradiol trial evidence does not transfer to it. The randomized results behind estradiol come from specific FDA-approved gels, patches, tablets and vaginal products, each tested at defined strengths against placebo in defined populations, and each manufactured under the review that established its strength, purity and delivery. A compounded cream containing estradiol is not those products and cannot claim their results. Compounded preparations are not reviewed by the FDA for safety, effectiveness or quality.4
There is no FDA-approved drug containing estriol, so half the formula has no labeling.
The detail
Half of this formula has no approved product to reason from. The FDA states that there are no FDA-approved drugs containing estriol, that marketed drugs containing estriol are compounded drugs which are not FDA-approved, and that it does not have evidence that drugs containing estriol are safe and effective or are safer forms of estrogen. There is therefore no approved labeling, no established dose and no approved-product safety database for the estriol component.4
There are too few trials to assess breast cancer, endometrial cancer or cardiovascular risk.
The detail
The safety questions here are open, not answered. The same meta-analysis that found no adverse metabolic signal concluded explicitly that there are insufficient randomized trials of compounded bioidentical hormone therapy to assess the clinical risk of breast cancer, endometrial cancer or cardiovascular disease, and that clinical cardiovascular events, endometrial biopsy and breast cancer risk were not studied at all. Absence of evidence is not evidence that the risks of the estrogen class stop applying to a compounded estrogen.12
- National Academies of Sciences, Engineering, and Medicine. The Clinical Utility of Compounded Bioidentical Hormone Therapy: A… Washington, DC: National Academies Press; 2020.DOI
- Liu Y, Yuan Y, Day AJ, Zhang W, John P, Ng DJ, Banov D. Safety and efficacy of compounded bioidentical hormone therapy (cBHT)… Menopause. 2022.
- The Writing Group for the PEPI Trial Effects of hormone replacement… JAMA. 1996.
- US Food and Drug Administration. Menopause. Consumer information on women's health topics, content current as of December 14, 2023.FDA
Important Safety Information
Boxed warning
The approved labeling for estradiol is therefore the best available guide to what this class does, and it carries a boxed warning that estrogen without a progestogen increases the risk of endometrial cancer in a woman who still has a uterus, so unopposed estrogen is not an appropriate plan in that situation and progesterone belongs in the conversation.
Do not use if you have
- A history of breast cancer or another estrogen-dependent cancer
- Unexplained vaginal bleeding
- A prior blood clot, stroke or heart attack
- An inherited clotting disorder
- Liver disease
- A known anaphylactic reaction, angioedema, or hypersensitivity to the product
- Pregnancy
Serious risks
- Stroke, deep vein thrombosis and pulmonary embolism
- Gallbladder disease
- Probable dementia in women who begin therapy at 65 or older
- Breast cancer when estrogen and a progestogen are taken together over longer use
- Compounding has not been shown to reduce any of them
Commonly reported
- Breast tenderness
- Irregular vaginal bleeding or spotting
- Headache
- Irritation where the cream is applied
Because it is a cream
- Estradiol applied to skin can transfer to another person through skin contact before it dries
Reported effects follow the estrogen class. This is a compounded preparation, which means it has not been reviewed by the FDA for safety, effectiveness, or quality, and estriol is not a component of any FDA-approved drug product, so there is no approved labeling for that half of the formula. A licensed provider decides whether an individualized preparation is the right call for your case, and a licensed 503A pharmacy prepares it only after that decision.
Questions
Asked and answered.
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