United States · FDA National Drug Code directory
MEDULTIMA ADVENTURE SUNSCREEN
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 84066-109_5368b2b3-fd81-9659-e063-6394a90a0ad3
- Product NDC
- 84066-109
- Form
- CREAM
- Composition / generic term
- Homosalate,Octocrylene, Phenylbenzimidazole Sulfonic Acid, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane
- Labeler
- Guangzhou Tata Biotechnology Co., Ltd.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20260604
- Source listing expiry
- 20271231
Source-listed 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
These values do not establish equivalence or a dose recommendation.
Packages
- 50 g in 1 BOTTLE (84066-109-01) · 84066-109-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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