Home NDC 81537-282 DMK Ultrascreen Mineral Sunscreen
Product NDC 81537-282
11-digit product format 815370282
Labeler code 81537
Product ID 81537-282_47e3612d-4c31-b24f-e063-6394a90a80f8
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Danne Montague King
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-24
Substance ZINC OXIDE
Active strength 132 mg/mL
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 DMK Ultrascreen Mineral Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 132 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 81537-282-01 DMK Ultrascreen Mineral Sunscreen 65 mL in 1 BOTTLE LOTION 65 2 81537-282-02 DMK Ultrascreen Mineral Sunscreen 1 in 1 CARTON LOTION 1 2
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 45 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 81537-282-01 81537028201 65 mL in 1 BOTTLE 65 ml Historical 81537-282-02 81537028202 1 BOTTLE in 1 CARTON (81537-282-02) / 65 mL in 1 BOTTLE (81537-282-01) 1 bottle 2025-04-24 No No Current