Home NDC 87250-001 Femarone 20
Product NDC 87250-001
11-digit product format 872500001
Labeler code 87250
Product ID 87250-001_44ea74ce-2ba2-e578-e063-6394a90ab72d
Type HUMAN OTC DRUG
Nonproprietary name Femarone 20
Dosage form CREAM
Route TRANSDERMAL
Labeler Wise Essentials LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-12-05
Substance PROGESTERONE
Active strength 20 mg/58g
Pharmacologic classes Progesterone [CS], Progesterone [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Femarone 20
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PROGESTERONE 20 mg/58g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4G7DS2Q64Y Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87250-001-11 Femarone 20 58 g in 1 JAR CREAM 58 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87250-001-11 87250000111 58 g in 1 JAR (87250-001-11) 58 g 2025-12-06 No No Current