Home NDC 84509-105 Sunscreen for baby SPF50plus
Product NDC 84509-105
11-digit product format 845090105
Labeler code 84509
Product ID 84509-105_4e784b54-ce43-c667-e063-6394a90a8679
Type HUMAN OTC DRUG
Nonproprietary name Octocrylene,Ethylhexyl Methoxycinnamate,Titanium Dioxide,Ethylhexyl Salicylate
Dosage form LOTION
Route TOPICAL
Labeler Guangzhou Senmai Biotechnology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-02
Substance OCTOCRYLENE; TITANIUM DIOXIDE; OCTINOXATE; OCTISALATE
Active strength 3000; 2400; 3000; 1500 mg/30mL; mg/30mL; mg/30mL; mg/30mL
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 Sunscreen for baby SPF50plus
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 3000 mg/30mL TITANIUM DIOXIDE 2400 mg/30mL OCTINOXATE 3000 mg/30mL OCTISALATE 1500 mg/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 84509-105-01 Sunscreen for baby SPF50plus 30 mL in 1 BOTTLE LOTION 30 7
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 84509-105-01 84509010501 30 mL in 1 BOTTLE (84509-105-01) 30 ml 2026-04-02 No No Current