Wound Gel
- Product NDC
- 71521-037
- 11-digit product format
- 715210037
- Labeler code
- 71521
- Product ID
- 71521-037_da597081-3856-3ab7-e053-2995a90a7120
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Lavior Inc
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-31
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71521-037 | WOUND GEL (ALLANTOIN) GEL [LAVIOR PHARMA INC] | 8 | Legacy NDC | 20241024_bdd10ce8-1354-2d9a-e053-2a95a90ad848.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71521-037-15 | 71521003715 | 15 g in 1 TUBE (71521-037-15) | 15 g | 2022-03-17 | 0000-00-00 | No | No | Current |
| 71521-037-50 | 71521003750 | 50 g in 1 BOTTLE, PUMP (71521-037-50) | 50 g | 2021-03-31 | 0000-00-00 | No | No | Current |