HYDROQUINONE 4%
- Product NDC
- 72934-6114
- 11-digit product format
- 729346114
- Labeler code
- 72934
- Product ID
- 72934-6114_874bd64a-5af2-221e-e053-2995a90a6f79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROQUINONE 4%
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- Sincerus Florida, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-05-01
- Marketing end
- 0000-00-00
- Substance
- HYDROQUINONE
- Active strength
- 4 g/100g
- Pharmacologic classes
- Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Depigmenting Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72934-6114-2 | HYDROQUINONE 4% | 30 g in 1 BOTTLE, PUMP | EMULSION | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72934-6114 | HYDROQUINONE 4% EMULSION [SINCERUS FLORIDA, LLC] | 1 | Legacy NDC, 1 package rows | 20190501_874bd64a-5af1-221e-e053-2995a90a6f79.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72934-6114-2 | 72934611402 | 30 g in 1 BOTTLE, PUMP | 30 g | Historical |