Dr. Lightening Ultra-Potent Facial
- Product NDC
- 63742-025
- 11-digit product format
- 637420025
- Labeler code
- 63742
- Product ID
- 63742-025_87be89b9-81fc-5e5c-e053-2995a90a3f18
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HYDROQUINONE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Clinical Resolution Laboratory, Inc.
- Application
- part358A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-02-15
- Marketing end
- 0000-00-00
- Substance
- HYDROQUINONE
- Active strength
- 20 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63742-025-01 | 63742002501 | 44 g in 1 TUBE (63742-025-01) | 44 g | 2019-02-15 | 0000-00-00 | No | No | Current |