Home NDC 81679-211 Mineral Based Foam Sunscreen Non-Tinted
Product NDC 81679-211
11-digit product format 816790211
Labeler code 81679
Product ID 81679-211_457579a1-1b01-7cd4-e063-6294a90a2225
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-06-10
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 30; 100 mg/g; mg/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 Mineral Based Foam Sunscreen Non-Tinted
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 30 mg/g ZINC OXIDE 100 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup 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 81679-211-04 Mineral Based Foam Sunscreen Non-Tinted 100 g in 1 BOTTLE, DISPENSING AEROSOL, FOAM 100 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81679-211 MINERAL BASED FOAM SUNSCREEN NON-TINTED (TITANIUM DIOXIDE, ZINC OXIDE) AEROSOL, FOAM [KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION] 1 Current NDC, 1 package rows 20250410_32486bfb-0cc8-0283-e063-6394a90a9967.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 45 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81679-211-04 81679021104 100 g in 1 BOTTLE, DISPENSING (81679-211-04) 100 g 2021-06-10 No No Current