SPF 50 Mineral Based Facial Sunscreen
- Product NDC
- 81679-258
- 11-digit product format
- 816790258
- Labeler code
- 81679
- Product ID
- 81679-258_d1612c94-e50e-4ba5-a591-a7dfa77fb5f8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Hutton, Kathleen MD
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-03-25
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 100; 30 mg/g; 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
- SPF 50 Mineral Based Facial Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TITANIUM DIOXIDE | 100 mg/g |
| ZINC OXIDE | 30 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 15FIX9V2JP, SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81679-258-50 | SPF 50 Mineral Based Facial Sunscreen | 53 g in 1 BOTTLE, PUMP | CREAM | 53 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81679-258 | SPF 50 MINERAL BASED FACIAL SUNSCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [HUTTON, KATHLEEN MD] | 1 | Current NDC, 1 package rows | 20240329_5cf0d2e3-d496-424c-ac75-70ff5b87e9ca.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 81679-258-50 | 81679025850 | 53 g in 1 BOTTLE, PUMP (81679-258-50) | 53 g | 2024-03-25 | No | No | Current |