Home NDC 85533-203 Tinted Matte Defense Sunscreen Primer
Product NDC 85533-203
11-digit product format 855330203
Labeler code 85533
Product ID 85533-203_45b4d122-1d1f-1945-e063-6294a90a90bb
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler Mint Skin Incorporated
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-07-06
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 38; 80 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 Tinted Matte Defense Sunscreen Primer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 38 mg/g TITANIUM DIOXIDE 80 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP 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 85533-203-15 Tinted Matte Defense Sunscreen Primer 1.5 g in 1 PACKET CREAM 1.5 2 85533-203-50 Tinted Matte Defense Sunscreen Primer 53 g in 1 BOTTLE, PUMP CREAM 53 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85533-203 TINTED MATTE DEFENSE SUNSCREEN PRIMER (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [MINT SKIN INCORPORATED] 1 Current NDC, 1 package rows 20250516_352f8de3-8ff0-4098-e063-6294a90ace4d.zip 85533-203 TINTED MATTE DEFENSE SUNSCREEN PRIMER (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [MINT SKIN INCROPORATED] 1 Current NDC, 1 package rows 20250516_35305bf1-8947-f275-e063-6294a90a3024.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 361 · 7,213 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85533-203-15 85533020315 1.5 g in 1 PACKET (85533-203-15) 1.5 g 2021-07-06 Yes No Current 85533-203-50 85533020350 53 g in 1 BOTTLE, PUMP (85533-203-50) 53 g 2021-07-06 No No Current