Home NDC 84066-109 MEDULTIMA ADVENTURE SUNSCREEN
Product NDC 84066-109
11-digit product format 840660109
Labeler code 84066
Product ID 84066-109_5368b2b3-fd81-9659-e063-6394a90a0ad3
Type HUMAN OTC DRUG
Nonproprietary name Homosalate,Octocrylene, Phenylbenzimidazole Sulfonic Acid, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane
Dosage form CREAM
Route TOPICAL
Labeler Guangzhou Tata Biotechnology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-04
Substance OCTOCRYLENE; ETHYLHEXYL SALICYLATE; PHENYLBENZIMIDAZOLE SULFONIC ACID; BUTYL METHOXYDIBENZOYLMETHANE; HOMOSALATE
Active strength 7; 4; 4; 3; 9 g/100g; g/100g; g/100g; g/100g; g/100g
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 MEDULTIMA ADVENTURE SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 7 g/100g ETHYLHEXYL SALICYLATE 4 g/100g PHENYLBENZIMIDAZOLE SULFONIC ACID 4 g/100g BUTYL METHOXYDIBENZOYLMETHANE 3 g/100g HOMOSALATE 9 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 27 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 84066-109-01 84066010901 50 g in 1 BOTTLE (84066-109-01) 50 g 2026-06-04 No No Current