sunscreen powder
- Product NDC
- 83447-001
- 11-digit product format
- 834470001
- Labeler code
- 83447
- Product ID
- 83447-001_479edb42-9157-566b-e063-6394a90a9101
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sunscreen powder
- Dosage form
- POWDER
- Route
- CUTANEOUS
- Labeler
- Guangzhou Fantesy Biotechnology Co.,Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-05-05
- Substance
- ZINC OXIDE
- Active strength
- 25 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- sunscreen powder
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 25 g/100g |
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 |
|---|
| 83447-001-01 | sunscreen powder | 3.5 g in 1 BOX | POWDER | 3.5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83447-001 | SUNSCREEN POWDER POWDER [GUANGZHOU FANTESY BIOTECHNOLOGY CO.,LTD] | 2 | Current NDC, 1 package rows | 20241122_fae8ecaf-7a9c-902b-e053-6394a90a5f31.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83447-001-01 | 83447000101 | 3.5 g in 1 BOX (83447-001-01) | 3.5 g | 2023-05-05 | No | No | Historical |