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- Product NDC
- 60716-080
- 11-digit product format
- 607160080
- Labeler code
- 60716
- Product ID
- 60716-080_ae7b7b8b-8094-47d1-bb24-6d8d14e5e0b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Caregen Co.,Ltd.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-06-01
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 0 g/10mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60716-080-02 | 60716008002 | 1 CONTAINER in 1 CARTON (60716-080-02) > 10 mL in 1 CONTAINER (60716-080-01) | 1 container | 2017-06-01 | 0000-00-00 | No | No | Current |