RENEWALUXE SPF 50 Sunscreen
- Product NDC
- 83447-005
- 11-digit product format
- 834470005
- Labeler code
- 83447
- Product ID
- 83447-005_47b31ef5-e027-ed4b-e063-6294a90a2d30
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- RENEWALUXE SPF 50 Sunscreen
- Dosage form
- CREAM
- Route
- CUTANEOUS
- Labeler
- Guangzhou Fantesy Biotechnology Co.,Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-06-26
- Substance
- ZINC OXIDE
- Active strength
- 21.8 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- RENEWALUXE SPF 50 Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 21.8 g/100mL |
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 |
|---|
| 83447-005-01 | RENEWALUXE SPF 50 Sunscreen | 50 mL in 1 BOX | CREAM | 50 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83447-005 | RENEWALUXE SPF 50 SUNSCREEN CREAM [GUANGZHOU FANTESY BIOTECHNOLOGY CO.,LTD] | 3 | Current NDC, 1 package rows | 20240810_1bc29960-5e73-e8ab-e063-6294a90a3f80.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83447-005-01 | 83447000501 | 50 mL in 1 BOX (83447-005-01) | 50 ml | 2024-06-26 | No | No | Historical |