Home NDC 85431-211 Foam Weightless Sunscreen Non-Tinted Drytouch NT
Product NDC 85431-211
11-digit product format 854310211
Labeler code 85431
Product ID 85431-211_45870c56-4bcf-5c3b-e063-6394a90a085c
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler Cutis Wellness Dermatology And Dermatopathology PLLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-03-15
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 Foam Weightless Sunscreen Non-Tinted Drytouch NT
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 85431-211-04 Foam Weightless Sunscreen Non-Tinted Drytouch NT 113 g in 1 BOTTLE, PUMP AEROSOL, FOAM 113 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85431-211 FOAM WEIGHTLESS SUNSCREEN NON-TINTED DRYTOUCH NT (TITANIUM DIOXIDE, ZINC OXIDE) AEROSOL, FOAM [CUTIS WELLNESS DERMATOLOGY AND DERMATOPATHOLOGY PLLC] 1 Current NDC, 1 package rows 20250424_335ec22c-6a9a-c4d1-e063-6394a90ac0b0.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 26 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 85431-211-04 85431021104 113 g in 1 BOTTLE, PUMP (85431-211-04) 113 g 2023-03-15 No No Current