CVS SPF 50 Face Sunscreen
- Product NDC
- 51316-217
- 11-digit product format
- 513160217
- Labeler code
- 51316
- Product ID
- 51316-217_3ef5b095-2666-ab5c-e063-6294a90aca85
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- CVS
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-28
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 6; 5 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
- CVS SPF 50 Face Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TITANIUM DIOXIDE | 6 g/100mL |
| ZINC OXIDE | 5 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 15FIX9V2JP, SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51316-217-01 | CVS SPF 50 Face Sunscreen | 50 mL in 1 BOTTLE | LOTION | 50 | | 2 |
| 51316-217-01 | CVS SPF 50 Face Sunscreen | 1 in 1 BOX | LOTION | 1 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51316-217-01 | 51316021701 | 1 BOTTLE in 1 BOX (51316-217-01) / 50 mL in 1 BOTTLE | 1 bottle | 2025-01-28 | No | No | Current |