HYDROQUINONE 4%
- Product NDC
- 50268-343
- 11-digit product format
- 502680343
- Labeler code
- 50268
- Product ID
- 50268-343_d5dd559f-ed86-5731-e053-2a95a90a1477
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroquinone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- AvPAK
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-11-23
- Marketing end
- 0000-00-00
- Substance
- HYDROQUINONE
- Active strength
- 40 mg/g
- Pharmacologic classes
- Depigmenting Activity [PE], Melanin Synthesis Inhibitor [EPC], Melanin Synthesis Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50268-343-28 | 50268034328 | 1 TUBE in 1 CARTON (50268-343-28) > 28.35 g in 1 TUBE | 1 tube | 2020-11-23 | 0000-00-00 | No | No | Current |