Allantoin
- Product NDC
- 30142-195
- 11-digit product format
- 301420195
- Labeler code
- 30142
- Product ID
- 30142-195_c78ec7ad-f520-b856-e053-2a95a90ad90a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Advanced Derma Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Kroger Co.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-02-12
- 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 |
|---|
| 30142-195-85 | 30142019585 | 85 g in 1 CAN (30142-195-85) | 85 g | 2018-02-12 | 0000-00-00 | No | No | Current |