DailyMed label
MEDULTIMA ADVENTURE SUNSCREEN
DailyMed label · Guangzhou Tata Biotechnology Co., Ltd. · version 1
Key facts
| Product | MEDULTIMA ADVENTURE SUNSCREEN |
|---|---|
| Labeler | Guangzhou Tata Biotechnology Co., Ltd. |
| Document type | HUMAN OTC DRUG LABEL |
| Active ingredients | BUTYL METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE, HOMOSALATE, OCTOCRYLENE, PHENYLBENZIMIDAZOLE SULFONIC ACID |
| Active ingredient UNIIs | 4X49Y0596W, 5A68WGF6WM, 9YQ9DI1W42, G63QQF2NOX, V06SV4M95S |
| Application number | M020 |
| Route | TOPICAL |
| NDC package codes | 84066-109-01 |
| Effective date | Jun 4, 2026 |
| Set ID | 5368b2b3-fd80-9659-e063-6394a90a0ad3 |
At a glance
- 1–9 NDC package codes
- 1–9 Active ingredients
- 1–9 Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: