Allantoin
- Product NDC
- 59779-423
- 11-digit product format
- 597790423
- Labeler code
- 59779
- Product ID
- 59779-423_c740f7c1-04d2-1785-e053-2995a90ae118
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Advanced Derma Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- CVS Pharmacy
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-04-15
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 0 g/85g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59779-423-85 | 59779042385 | 85 g in 1 CAN (59779-423-85) | 85 g | 2015-04-15 | 0000-00-00 | No | No | Current |