Home NDC 85248-137 Beilloso Women Estriol
Product NDC 85248-137
11-digit product format 852480137
Labeler code 85248
Product ID 85248-137_4a71973a-27be-5016-e063-6394a90a39a7
Type HUMAN OTC DRUG
Nonproprietary name Micronized Estriol 0.1% Women Estriol
Dosage form CREAM
Route TOPICAL
Labeler Jiangxi Yudexi Pharmaceutical Co., LTD
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-02-10
Substance ESTRIOL
Active strength .1 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Beilloso Women Estriol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ESTRIOL .1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination FB33469R8E 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 85248-137-01 Beilloso Women Estriol 30 mL in 1 BOTTLE CREAM 30 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 85248-137-01 85248013701 30 mL in 1 BOTTLE (85248-137-01) 30 ml 2026-02-10 No No Current