Allantoin
- Product NDC
- 56104-034
- 11-digit product format
- 561040034
- Labeler code
- 56104
- Product ID
- 56104-034_c74070f8-d298-4f5c-e053-2995a90ad110
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Advanced Derma Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-03-27
- Marketing end
- 2021-12-31
- Substance
- ALLANTOIN
- Active strength
- 0 g/85g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 56104-034-85 | 56104003485 | 85 g in 1 CAN (56104-034-85) | 85 g | 2018-03-27 | 2021-12-31 | No | No | Current |