Home NDC 72476-920 Zinc Oxide
Product NDC 72476-920
11-digit product format 724760920
Labeler code 72476
Product ID 72476-920_5940399c-31e4-6d51-e063-6294a90a8e7c
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form PASTE
Route TOPICAL
Labeler ADUSA Distribution, LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-17
Substance ZINC OXIDE
Active strength 400 mg/g
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 Zinc Oxide
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 400 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1094560 Internal RxNorm 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 28 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72476-920-26 72476092026 1 TUBE in 1 CARTON (72476-920-26) / 113 g in 1 TUBE 1 tube 2026-08-17 No No Current