Hydroquinone
- Product NDC
- 24979-141
- 11-digit product format
- 249790141
- Labeler code
- 24979
- Product ID
- 24979-141_a7823404-84c7-4040-a543-5d9edf440b79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroquinone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- TWi Pharmaceuticals, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-06-16
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 24979-141-36 | 24979014136 | 1 TUBE in 1 CARTON (24979-141-36) > 28.35 g in 1 TUBE | 1 tube | 2017-06-16 | 0000-00-00 | No | No | Current |