Home NDC 84938-005 SUNSCREEN Stick
Product NDC 84938-005
11-digit product format 849380005
Labeler code 84938
Product ID 84938-005_460e1038-30f1-a6e4-e063-6394a90ad534
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide 15%, Titanium Dioxide 8%, Homosalate 6%
Dosage form STICK
Route TOPICAL
Labeler Foshan Sugar Max Cosmetics CO.,Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-16
Substance TITANIUM DIOXIDE; HOMOSALATE; ZINC OXIDE
Active strength .08; .06; .15 g/g; g/g; g/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 SUNSCREEN Stick
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE .08 g/g HOMOSALATE .06 g/g ZINC OXIDE .15 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup V06SV4M95S Internal UNII lookup 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 84938-005-01 SUNSCREEN Stick 75 g in 1 CARTON STICK 75 1
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 84938-005-01 84938000501 75 g in 1 CARTON (84938-005-01) 75 g 2025-12-16 No No Current