Home NDC 74458-238 LYOPHILIZED AMNION WITH ALBUMIN
Product NDC 74458-238
11-digit product format 744580238
Labeler code 74458
Product ID 74458-238_580de9cc-bae7-fb1b-e063-6394a90ad74c
Type HUMAN OTC DRUG
Nonproprietary name HUMAN AMNIOTIC MEMBRANE
Dosage form POWDER, FOR SOLUTION
Route TOPICAL
Labeler Guangzhou Yilong Cosmetics.,Ltd
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-11
Substance HUMAN AMNIOTIC MEMBRANE
Active strength 2 mg/100mg
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 LYOPHILIZED AMNION WITH ALBUMIN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HUMAN AMNIOTIC MEMBRANE 2 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination T9O10FB50M 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 8 of 36 · 719 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 74458-238-01 74458023801 10 mg in 1 BOTTLE (74458-238-01) 10 mg 2026-07-30 No No Current