Home NDC 85727-204 Mineral Sunscreen Tinted Zinc Oxide
Product NDC 85727-204
11-digit product format 857270204
Labeler code 85727
Product ID 85727-204_45c735c9-d906-0e7a-e063-6394a90ac08d
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler KS Esthetics, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-01
Substance ZINC OXIDE
Active strength 200 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 Mineral Sunscreen Tinted Zinc Oxide
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 200 mg/g
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 85727-204-60 Mineral Sunscreen Tinted Zinc Oxide 60 g in 1 BOTTLE, PUMP CREAM 60 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 26 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85727-204-60 85727020460 60 g in 1 BOTTLE, PUMP (85727-204-60) 60 g 2019-04-01 No No Current