SUNSCREEN SPF50
- Product NDC
- 85998-001
- 11-digit product format
- 859980001
- Labeler code
- 85998
- Product ID
- 85998-001_3bc1c6e9-1dd6-d7c6-e063-6394a90ad89e
- 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
- Marketing start
- 2025-08-07
- Substance
- ETHYLHEXYL METHOXYCINNAMATE; OCTOCRYLENE; TITANIUM DIOXIDE
- Active strength
- 6; 4; 2 g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SUNSCREEN SPF50
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ETHYLHEXYL METHOXYCINNAMATE | 6 g/100mL |
| OCTOCRYLENE | 4 g/100mL |
| TITANIUM DIOXIDE | 2 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4Y5P7MUD51, 5A68WGF6WM, 15FIX9V2JP |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85998-001-01 | SUNSCREEN SPF50 | 50 mL in 1 BOTTLE | CREAM | 50 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85998-001-01 | 85998000101 | 50 mL in 1 BOTTLE (85998-001-01) | 50 ml | 2025-08-07 | No | No | Current |