Home NDC 54136-351 Mineral Sunscreen SPF 50
Product NDC 54136-351
11-digit product format 541360351
Labeler code 54136
Product ID 54136-351_5dd63829-942f-d0f2-e063-6394a90a4c55
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler Better Planet Brands LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-01
Substance ZINC OXIDE
Active strength 22 g/100g
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 Mineral Sunscreen SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 22 g/100g
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 54136-351-92 Mineral Sunscreen SPF 50 92 g in 1 TUBE CREAM 92 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 54136-351 MINERAL SUNSCREEN SPF 50 (ZINC OXIDE) CREAM [BETTER PLANET BRANDS LLC] 3 Current NDC, 1 package rows 20250130_1d8e727c-8b50-9cf2-e063-6394a90a2e15.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 162 of 353 · 7,049 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 54136-351-92 54136035192 92 g in 1 TUBE (54136-351-92) 92 g 2024-02-01 No No Current