Skin Lightener
- Product NDC
- 68723-142
- 11-digit product format
- 687230142
- Labeler code
- 68723
- Product ID
- 68723-142_4b795804-92d5-4cd0-9747-8b510e3be5ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroquinone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Axia Medical Solutions, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1990-12-01
- 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
- 2022-12-31
- 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 |
|---|
| 68723-142-02 | Skin Lightener | 1 in 1 BOX | CREAM | 1 | | 3 |
| 68723-142-02 | Skin Lightener | 57 g in 1 BOTTLE | CREAM | 57 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68723-142 | SKIN LIGHTENER (HYDROQUINONE) CREAM [AXIA MEDICAL SOLUTIONS, LLC] | 3 | Legacy NDC, 2 package rows | 20210220_9095eba6-6e02-4689-92f3-3ac73cd58f63.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68723-142-02 | 68723014202 | 1 BOTTLE in 1 BOX (68723-142-02) > 57 g in 1 BOTTLE | 1 bottle | 1990-12-01 | 0000-00-00 | No | No | Current |