Home NDC 72667-101 SPF 50 Mineral Sunscreen
Product NDC 72667-101
11-digit product format 726670101
Labeler code 72667
Product ID 72667-101_374d7396-31f7-8fd6-e063-6394a90ab10e
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Inspec Solutions, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-03
Substance ZINC OXIDE
Active strength 20 g/100g
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 SPF 50 Mineral Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 20 g/100g
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 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 72667-101-01 SPF 50 Mineral Sunscreen 50 g in 1 TUBE LOTION 50 2 72667-101-02 SPF 50 Mineral Sunscreen 177 g in 1 TUBE LOTION 177 2
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 78 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72667-101-01 72667010101 50 g in 1 TUBE (72667-101-01) 50 g 2025-06-03 No No Current 72667-101-02 72667010102 177 g in 1 TUBE (72667-101-02) 177 g 2025-06-03 No No Current