BRIGHTEN
- Product NDC
- 54272-301
- 11-digit product format
- 542720301
- Labeler code
- 54272
- Product ID
- 54272-301_2d9bf516-a130-4aaf-8efb-600250a7236d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HYDROQUINONE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- CEN BEAUTY LLC
- Application
- part358A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-02-21
- Marketing end
- 0000-00-00
- Substance
- HYDROQUINONE
- Active strength
- 2 g/100mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 54272-301-11 | BRIGHTENLIGHTENING | 30 mL in 1 TUBE | GEL | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54272-301 | BRIGHTEN LIGHTENING (HYDROQUINONE) GEL [CEN BEAUTY LLC] | 1 | Legacy NDC, 1 package rows | 20130306_c4f30486-d2ae-403c-9113-3f2a5b1476d5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 54272-301-11 | 54272030111 | 30 mL in 1 TUBE | 30 ml | Historical |