Home NDC 79009-902 OMIC MINERAL SUNSCREEN
Product NDC 79009-902
11-digit product format 790090902
Labeler code 79009
Product ID 79009-902_5d43e4bd-24e5-7c16-e063-6294a90afbf8
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler Mitchell Cosmetics, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-02
Substance ZINC OXIDE
Active strength .18 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 OMIC MINERAL SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE .18 g/g
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79009-902-80 OMIC MINERAL SUNSCREEN 1 g in 1 BOTTLE, DISPENSING LOTION 1 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 242 of 353 · 7,041 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79009-902-80 79009090280 1 g in 1 BOTTLE, DISPENSING (79009-902-80) 1 g 2026-03-02 No No Current