FDA NDC Directory · JSON-LD · Markdown

MEDULTIMA ADVENTURE SUNSCREEN

NDC 84066-109 · HUMAN OTC DRUG · CREAM

Generic nameHomosalate,Octocrylene, Phenylbenzimidazole Sulfonic Acid, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane
Labeler / ManufacturerGuangzhou Tata Biotechnology Co., Ltd.
Marketing categoryOTC monograph drug · App M020
Dosage form / routeCREAM · TOPICAL
Active ingredientsOCTOCRYLENE (7 g/100g)
ETHYLHEXYL SALICYLATE (4 g/100g)
PHENYLBENZIMIDAZOLE SULFONIC ACID (4 g/100g)
BUTYL METHOXYDIBENZOYLMETHANE (3 g/100g)
HOMOSALATE (9 g/100g)
Marketing started20260604
Package count1

External sources

Source: openFDA. Public-domain (CC0).