Home NDC 84938-015 Sunscreen Stick
Product NDC 84938-015
11-digit product format 849380015
Labeler code 84938
Product ID 84938-015_4637503c-46dd-68de-e063-6394a90abdc7
Type HUMAN OTC DRUG
Nonproprietary name Homosalate 15%, Octisallate 5%, Ensulizole 4%
Dosage form STICK
Route TOPICAL
Labeler Foshan Sugar Max Cosmetics CO.,Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-18
Substance OCTISALATE; ENSULIZOLE; HOMOSALATE
Active strength .06; .05; .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 OCTISALATE .06 g/g ENSULIZOLE .05 g/g HOMOSALATE .15 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup 9YQ9DI1W42 Internal UNII lookup V06SV4M95S 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 84938-015-01 Sunscreen Stick 75 g in 1 BOTTLE 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 84938-015-01 84938001501 75 g in 1 BOTTLE (84938-015-01) 75 g 2025-12-18 No No Current