Femarone 20 by Wise Essentials LLC FEMARONE 20 cream

Femarone 20 by

Drug Labeling and Warnings

Femarone 20 by is a Otc medication manufactured, distributed, or labeled by Wise Essentials LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Micronized Progesterone USP, (Wild Yam) 2%

DISCLAIMER

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs For further information about unapproved drugs, https://www.fda.gov/drugs/enforcement-activities-fda/unapproved-drugs

PURPOSE

This is a topical cream that contains bio-identical micronized USP progesterone derived from wild yam, blended with phytoestrogens. When applied topically to the skin, it may help to balance your hormones, and also to provide support for peri menopause and menopausal symptoms.

INDICATIONS AND USAGE

USES: This is a topical cream that contains bio-identical micronized USP progesterone derived from wild yam, blended with phytoestrogens. When applied topically to the skin, it may help to balance your hormones and also to provide support for perimenopause and menopause.

Apply once or twice a day. Massage into wrists, inner arms, thighs, chest, or apply or use as directed by your physician.

PREGNANCY OR BREASTFEEDING

If pregnant or nursing or if you have a serious medical condition, consult a healthcare professional before using this product.

KEEP OUT OF REACH OF CHILDREN

Keep out of Reach of Children.

DOSAGE & ADMINISTRATION

Apply once or twice a day. Massage into wrists, inner arms, thighs, chest, or apply to together or use as directed by your physician.

INACTIVE INGREDIENT

Water, Wild Yam Extract, Chaste Tree Berry, Coconut Oil Organic, Vegetable Glycerin USP, Emulsifying Wax NF, Olivem 1000, Glyceryl Stearate, Radish Root Extract, Aloe Vera Powder Organic, Jojoba Oil Organic, Allantoin, Shea Butter Organic

QUESTIONS?

QUESTIONS?

Contact support@wiseessentials.com

SAFETY

Report Adverse Events click here https://www.accessdata.fda.gov/scripts/medwatch/

FDA Safety Recalls Click here https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Presence in Breast Milk Click here https://www.ncbi.nlm.nih.gov/books/NBK501345/

RELATED RESOURCES

Medline Plus. Click here https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=PROGESTERONE&_gl=1*f9papn*_ga*MTc2NTIwMjU3MS4xNzY1Njc2NTE5*_ga_7147EPK006*czE3NjU2NzY1MTgkbzEkZzEkdDE3NjU2NzY4NzEkajI1JGwwJGgw*_ga_P1FPTH9PL4*czE3NjU2NzY1MTgkbzEkZzEkdDE3NjU2NzY4NzEkajI1JGwwJGgw

Clinical Trials.Click here https://www.clinicaltrials.gov/search?term=PROGESTERONE&viewType=Table#classicRedirect

Biochemcical Date Summary. Click here. https://go.drugbank.com/drugs/DB00396

WARNINGS

WARNINGS: If pregnant or nursing or if you have a serious medical condition, consult a healthcare professional before using this product.
KEEP OUT OF REACH OF CHILDREN Store in a cool, dry place
Always consult your healthcare provider before using or if pregnant or nursing. Cease use and seek medical attention if skin irritation or a negative reaction.
Keep out of reach of children. Store in a cool, dry place.
California Prop 65 Law requires this statement: This product contains progesterone,
a chemical known only to the State of California to cause cancer. Cease using this product
and seek medical attention if skin irritation or other negative reactions occur.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FEMARONE 20 
femarone 20 cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87250-001
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y)	PROGESTERONE	20 mg  in 58 g

Inactive Ingredients
Ingredient Name	Strength
CHASTE TREE FRUIT (UNII: 433OSF3U8A)	2.5 mg  in 58 g
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)	40 mg  in 58 g
JOJOBA OIL (UNII: 724GKU717M)	5 mg  in 58 g
GLYCERIN (UNII: PDC6A3C0OX)	30 mg  in 58 g
SORBITAN OLIVATE (UNII: MDL271E3GR)	20 mg  in 58 g
DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)	80 mg  in 58 g
ALLANTOIN (UNII: 344S277G0Z)	2.5 mg  in 58 g
RADISH (UNII: EM5RP35463)	2.5 mg  in 58 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87250-001-11	58 g in 1 JAR; Type 0: Not a Combination Product	12/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/05/2025

Labeler - Wise Essentials LLC (080921731)