SUNSCREEN
- Product NDC
- 62932-168
- 11-digit product format
- 629320168
- Labeler code
- 62932
- Product ID
- 62932-168_79a30211-a454-191a-e053-2991aa0a90d6
- 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
- 2018-12-31
- 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 |
|---|
| 62932-168-20 | SUNSCREEN | 84 g in 1 TUBE | OINTMENT | 84 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62932-168 | SUNSCREEN (ZINC OXIDE SUNSCREEN) OINTMENT [PRIVATE LABEL SELECT LTD CO] | 1 | Legacy NDC, 1 package rows | 20181231_79a30211-a453-191a-e053-2991aa0a90d6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62932-168-20 | 62932016820 | 84 g in 1 TUBE | 84 g | Historical |