Home NDC 75936-666 Mineral Mattescreen SPF 40 - Untinted
Product NDC 75936-666
11-digit product format 759360666
Labeler code 75936
Product ID 75936-666_536f483b-00ca-45aa-e063-6294a90a4ffd
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Supergoop, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-15
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 17.68; 1.33 g/100mL; g/100mL
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 Mattescreen SPF 40 - Untinted
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 17.68 g/100mL TITANIUM DIOXIDE 1.33 g/100mL
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.
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 75936-666-02 75936066602 1 TUBE in 1 BOX (75936-666-02) / 45 mL in 1 TUBE (75936-666-01) 1 tube 2026-01-15 No No Current 75936-666-03 75936066603 15 mL in 1 TUBE (75936-666-03) 15 ml 2026-01-15 No No Current 75936-666-04 75936066604 10 mL in 1 TUBE (75936-666-04) 10 ml 2026-01-15 Yes No Current