Activated Mineral Sunscreen Tinted
- Product NDC
- 83083-002
- 11-digit product format
- 830830002
- Labeler code
- 83083
- Product ID
- 83083-002_452053bf-8b70-6550-e063-6294a90a23be
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Activated Mineral Sunscreen Tinted
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Reve Skincare LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-03-25
- Substance
- ZINC OXIDE
- Active strength
- 142.8 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Activated Mineral Sunscreen Tinted
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 142.8 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83083-002-50 | Activated Mineral Sunscreen Tinted | 1 in 1 CARTON | CREAM | 1 | | 2 |
| 83083-002-50 | Activated Mineral Sunscreen Tinted | 50 mL in 1 TUBE | CREAM | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83083-002 | ACTIVATED MINERAL SUNSCREEN TINTED CREAM [REVE SKINCARE LLC] | 1 | Current NDC, 2 package rows | 20250327_312a32a7-d253-f10c-e063-6294a90a803a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83083-002-50 | 83083000250 | 1 TUBE in 1 CARTON (83083-002-50) / 50 mL in 1 TUBE | 1 tube | 2025-03-25 | No | No | Current |