SUNSCREEN SPF50
- Product NDC
- 85998-001
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYLHEXYL METHOXYCINNAMATE, OCTOCRYLENE, TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Guangzhou Tinsun Biotechnology Company Limited
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Substance
- ETHYLHEXYL METHOXYCINNAMATE; OCTOCRYLENE; TITANIUM DIOXIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 85998-001-01 | 50 mL in 1 BOTTLE (85998-001-01) | 2025-08-07 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 85998-001 SUNSCREEN SPF50 | Guangzhou Tinsun Biotechnology Company Limited | 2025-08-07 | HUMAN OTC DRUG LABEL | 1 |