Tinted Daily Protection Sunscreen
- Product NDC
- 85711-208
- 11-digit product format
- 857110208
- Labeler code
- 85711
- Product ID
- 85711-208_461546fa-70f5-dad0-e063-6394a90a4675
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Kemmi Lee Skin Science
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-04-02
- Substance
- ZINC OXIDE
- Active strength
- 160 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tinted Daily Protection Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 160 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85711-208-50 | Tinted Daily Protection Sunscreen | 50 g in 1 BOTTLE, PUMP | CREAM | 50 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85711-208-50 | 85711020850 | 50 g in 1 BOTTLE, PUMP (85711-208-50) | 50 g | 2024-04-02 | No | No | Historical |