Pure velocity SUNSCREEN SPF 50
- Product NDC
- 60771-0031
- 11-digit product format
- 607710031
- Labeler code
- 60771
- Product ID
- 60771-0031_40024b26-6118-7bae-e063-6294a90a33eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYLHEXYL METHOXYCINNAMATE,ZINC OXIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Haishi Biological Technology Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-30
- Substance
- ETHYLHEXYL METHOXYCINNAMATE; ZINC OXIDE
- Active strength
- 1.5; 3 g/100g; g/100g
- 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 |
|---|
| ETHYLHEXYL METHOXYCINNAMATE | 1.5 g/100g |
| ZINC OXIDE | 3 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4Y5P7MUD51, SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60771-0031-1 | Pure velocity SUNSCREEN SPF 50 | 30 g in 1 BOTTLE | LIQUID | 30 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60771-0031-1 | 60771003101 | 30 g in 1 BOTTLE (60771-0031-1) | 30 g | 2025-09-30 | No | No | Historical |