Glytone Skin Lightening
- Product NDC
- 64760-701
- 11-digit product format
- 647600701
- Labeler code
- 64760
- Product ID
- 64760-701_a5f13ce4-dfb2-5565-e053-2a95a90a50dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroquinone
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Pierre Fabre USA Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2010-04-01
- Marketing end
- 2022-04-30
- Substance
- HYDROQUINONE
- Active strength
- 40 mg/g
- Pharmacologic classes
- Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Depigmenting Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64760-701-01 | 64760070101 | 1 BOTTLE, PLASTIC in 1 CARTON (64760-701-01) > 56 g in 1 BOTTLE, PLASTIC | 2010-04-01 | 2022-04-30 | No | No | Current |