# MEDULTIMA ADVENTURE SUNSCREEN

NDC: 84066-109
Generic name: Homosalate,Octocrylene, Phenylbenzimidazole Sulfonic Acid, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane
Labeler / Manufacturer: Guangzhou Tata Biotechnology Co., Ltd.
Product type: HUMAN OTC DRUG
Marketing category: OTC monograph drug
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20260604

FDA application: M020

## Active ingredients

- OCTOCRYLENE: 7 g/100g
- ETHYLHEXYL SALICYLATE: 4 g/100g
- PHENYLBENZIMIDAZOLE SULFONIC ACID: 4 g/100g
- BUTYL METHOXYDIBENZOYLMETHANE: 3 g/100g
- HOMOSALATE: 9 g/100g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84066-109"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84066-109
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5368b2b3-fd80-9659-e063-6394a90a0ad3