FACIAL LIFTING
- Product NDC
- 69422-1001
- 11-digit product format
- 694221001
- Labeler code
- 69422
- Product ID
- 69422-1001_91cef68e-d363-37c3-e053-2a95a90a77b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLANTOIN
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- General Bio Co., Ltd.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-12-08
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record