Home NDC 72957-010 Matte Veil Tinted Broad Spectrum Sunscreen SPF 40
Product NDC 72957-010
11-digit product format 729570010
Labeler code 72957
Product ID 72957-010_5b31c901-0567-46d8-aac3-2377398d6414
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Titanium Dioxide
Dosage form CREAM
Route TOPICAL
Labeler Private Label Skin Care
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-01
Marketing end 2027-07-17
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 18; 1.5 g/100g; g/100g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
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 Matte Veil Tinted Broad Spectrum Sunscreen SPF 40 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 18 g/100g TITANIUM DIOXIDE 1.5 g/100g
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72957-010-01 Matte Veil Tinted Broad Spectrum Sunscreen SPF 40 51 g in 1 BOTTLE CREAM 51 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72957-010 MATTE VEIL TINTED BROAD SPECTRUM SUNSCREEN SPF 40 (ZINC OXIDE, TITANIUM DIOXIDE) CREAM [PRIVATE LABEL SKIN CARE] 1 Current NDC, 1 package rows 20250313_a8d60212-18a7-42af-8bb3-bfcff7690a49.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 Marketing end Sample Exclude flag Status 72957-010-01 72957001001 51 g in 1 BOTTLE (72957-010-01) 51 g 2025-01-01 2027-07-17 No No Historical