Pure velocity SUNSCREEN SPF 50
- Product NDC
- 60771-0038
- 11-digit product format
- 607710038
- Labeler code
- 60771
- Product ID
- 60771-0038_400611c9-c89e-4168-e063-6394a90a82dc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Guangzhou Haishi Biological Technology Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-30
- Substance
- HOMOSALATE; OCTINOXATE; OCTOCRYLENE
- Active strength
- 3.75; 3; 6 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
- Pure velocity SUNSCREEN SPF 50
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HOMOSALATE | 3.75 g/100mL |
| OCTINOXATE | 3 g/100mL |
| OCTOCRYLENE | 6 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V06SV4M95S, 4Y5P7MUD51, 5A68WGF6WM |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60771-0038-1 | Pure velocity SUNSCREEN SPF 50 | 75 mL in 1 BOTTLE | CREAM | 75 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60771-0038-1 | 60771003801 | 75 mL in 1 BOTTLE (60771-0038-1) | 75 ml | 2025-09-30 | No | No | Current |