Home NDC 87976-001 Estriora Cream
Product NDC 87976-001
11-digit product format 879760001
Labeler code 87976
Product ID 87976-001_5a53c026-aa7d-6c09-e063-6394a90a36e1
Type HUMAN OTC DRUG
Nonproprietary name Estriol and Estradiol Cream
Dosage form CREAM
Route TOPICAL
Labeler Guangzhou Shunfei Network Technology Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-31
Substance ESTRIOL; ESTRADIOL
Active strength .2; .01 g/100g; g/100g
Pharmacologic classes Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Estriora Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ESTRIOL .2 g/100g ESTRADIOL .01 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination FB33469R8E Internal UNII lookup 4TI98Z838E Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 87976-001-01 87976000101 30 g in 1 TUBE (87976-001-01) 30 g 2026-08-31 No No Current