SUNSCREEN
- Product NDC
- 62932-189
- 11-digit product format
- 629320189
- Labeler code
- 62932
- Product ID
- 62932-189_7be980eb-73bc-fd21-e053-2a91aa0af1d5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE SUNSCREEN
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Private Label Select Ltd CO
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-11-30
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 20 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62932-189-32 | SUNSCREEN | 15 g in 1 TUBE | OINTMENT | 15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62932-189 | SUNSCREEN (ZINC OXIDE SUNSCREEN) OINTMENT [PRIVATE LABEL SELECT LTD CO] | 1 | Legacy NDC, 1 package rows | 20181201_7be980eb-73bb-fd21-e053-2a91aa0af1d5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62932-189-32 | 62932018932 | 15 g in 1 TUBE | 15 g | Historical |