Home NDC 64772-201 Zinc Oxide
Product NDC 64772-201
11-digit product format 647720201
Labeler code 64772
Product ID 64772-201_37eff762-1eaa-ec66-e063-6394a90a3d10
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide Ointment
Dosage form OINTMENT
Route TOPICAL
Labeler Derma Sciences Canada Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-11-03
Substance ZINC OXIDE
Active strength .2 g/g
NDC exclude flag No
Listing certified through 2026-12-31
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 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE .2 g/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 198911 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64772-201-01 Zinc Oxide 453.6 g in 1 JAR OINTMENT 453.6 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 30 of 68 · 1,357 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 64772-201-01 64772020101 453.6 g in 1 JAR (64772-201-01) 453.6 g 2014-11-03 No No Current