Glytone SunVanish Skin Lightening
- Product NDC
- 64760-702
- 11-digit product format
- 647600702
- Labeler code
- 64760
- Product ID
- 64760-702_a5f17279-5e4f-8c28-e053-2a95a90a6691
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroquinone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Pierre Fabre USA Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-06-13
- Marketing end
- 2021-09-30
- Substance
- HYDROQUINONE; AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 40 mg/g; mg/g; mg/g; mg/g; 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64760-702-01 | 64760070201 | 1 TUBE in 1 CARTON (64760-702-01) > 56 g in 1 TUBE | 1 tube | 2018-03-14 | 2021-09-30 | No | No | Current |