Up and Up Advanced Scar
- Product NDC
- 11673-700
- 11-digit product format
- 116730700
- Labeler code
- 11673
- Product ID
- 11673-700_86be49cd-e9ea-2d47-e053-2991aa0a84c7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLANTOIN
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-08-01
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 5 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record