Home NDC 62742-4153 Mineral Sunscreen Moisturizer Broad Spectrum SPF 20
Product NDC 62742-4153
11-digit product format 627424153
Labeler code 62742
Product ID 62742-4153_00a92501-f7cc-4f23-9d10-56e102b7ad41
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide and Titanium Dioxide
Dosage form CREAM
Route TOPICAL
Labeler Allure Labs, Inc
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2017-12-12
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 48; 50 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Mineral Sunscreen Moisturizer Broad Spectrum SPF 20
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 48 mg/mL TITANIUM DIOXIDE 50 mg/mL
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 62742-4153-1 Mineral Sunscreen Moisturizer Broad Spectrum SPF 20 40 mL in 1 BOTTLE CREAM 40 1 62742-4153-2 Mineral Sunscreen Moisturizer Broad Spectrum SPF 20 1 in 1 CARTON CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62742-4153 MINERAL SUNSCREEN MOISTURIZER BROAD SPECTRUM SPF 20 (ZINC OXIDE AND TITANIUM DIOXIDE) CREAM [ALLURE LABS, INC] 1 Current NDC, Legacy NDC, 2 package rows 20171213_316c2132-ab81-47f6-8e80-71e9252a2663.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 1 of 1 · 1 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 62742-4153-1 62742415301 40 mL in 1 BOTTLE 40 ml Historical 62742-4153-2 62742415302 1 BOTTLE in 1 CARTON (62742-4153-2) / 40 mL in 1 BOTTLE (62742-4153-1) 1 bottle 2017-12-12 0000-00-00 No No Current