GLINT
- Product NDC
- 71486-3040
- 11-digit product format
- 714863040
- Labeler code
- 71486
- Product ID
- 71486-3040_7619ef15-5773-3ce6-e053-2a91aa0ac35e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- GLINT COSMETICS PRIVATE LIMITED
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-09-17
- 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 |
|---|
| 71486-3040-3 | GLINT | 28 g in 1 TUBE | OINTMENT | 28 | | 1 |
| 71486-3040-4 | GLINT | 56 g in 1 TUBE | OINTMENT | 56 | | 1 |
| 71486-3040-5 | GLINT | 425 g in 1 JAR | OINTMENT | 425 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71486-3040 | GLINT (ZINC OXIDE) OINTMENT [GLINT COSMETICS PRIVATE LIMITED] | 1 | Legacy NDC, 3 package rows | 20180918_7619ef15-5772-3ce6-e053-2a91aa0ac35e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71486-3040-3 | 71486304003 | 28 g in 1 TUBE | 28 g | Historical |
| 71486-3040-4 | 71486304004 | 56 g in 1 TUBE | 56 g | Historical |
| 71486-3040-5 | 71486304005 | 425 g in 1 JAR | 425 g | Historical |