Home NDC 69396-021-54 Zinc Oxide 20%
Product NDC 69396-021
Requested package NDC 69396-021-54
11-digit product format 693960021
Labeler code 69396
Product ID 69396-021_521c0f8d-c99e-0b87-e063-6294a90abdbc
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form OINTMENT
Route TOPICAL
Labeler Trifecta Pharmaceuticals USA
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-01-26
Substance ZINC OXIDE
Active strength .2 g/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 20%
Listing expiration 2027-12-31 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69396-021-54 Zinc Oxide 20% 1 in 1 JAR OINTMENT 1 9 69396-021-54 Zinc Oxide 20% 454 g in 1 JAR OINTMENT 454 9 69396-021-02 Zinc Oxide 20% 1 in 1 BOX OINTMENT 1 7 69396-021-02 Zinc Oxide 20% 60 g in 1 TUBE OINTMENT 60 7 69396-021-01 Zinc Oxide 20% 28 g in 1 TUBE OINTMENT 28 2 69396-021-01 Zinc Oxide 20% 1 in 1 BOX OINTMENT 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69396-021 ZINC OXIDE 20% (ZINC OXIDE) OINTMENT [TRIFECTA PHARMACEUTICALS USA] 8 Current NDC, Legacy NDC, 2 package rows 20241222_8cbe9b1f-fec0-9579-e053-2995a90ac461.zip 69396-021 ZINC OXIDE 20% (ZINC OXIDE) OINTMENT [TRIFECTA PHARMACEUTICALS USA] 4 Current NDC, Legacy NDC, 2 package rows 20250112_63b551fc-7d16-c099-e053-2a91aa0a5f2c.zip 69396-021 ZINC OXIDE 20% (ZINC OXIDE) OINTMENT [TRIFECTA PHARMACEUTICALS USA] 2 Current NDC, Legacy NDC, 2 package rows 20180126_61f5aefe-9b43-a616-e053-2a91aa0acdbc.zip
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 51 of 68 · 1,350 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69396-021-54 69396002154 1 JAR in 1 JAR (69396-021-54) / 454 g in 1 JAR 1 jar 2019-07-01 0000-00-00 No No Current