Home NDC 85558-204 Moisturizing Mineral Sunscreen Tinted
Product NDC 85558-204
11-digit product format 855580204
Labeler code 85558
Product ID 85558-204_4628608e-8b5e-3761-e063-6294a90ad522
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler LOTUS SKINCARE AND MAKE-UP STUDIO
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-21
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 Moisturizing Mineral Sunscreen Tinted
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 85558-204-60 Moisturizing Mineral Sunscreen Tinted 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 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 85558-204-60 85558020460 60 g in 1 BOTTLE, PUMP (85558-204-60) 60 g 2023-08-21 No No Current