Dark Spot Lightening Cream
- Product NDC
- 56152-4002
- 11-digit product format
- 561524002
- Labeler code
- 56152
- Product ID
- 56152-4002_7d8d68c1-a16c-29d3-e053-2991aa0a0563
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydroquinone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Cosmetic Enterprises Ltd.
- Application
- part358A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-12-21
- Marketing end
- 0000-00-00
- Substance
- HYDROQUINONE
- Active strength
- 2 g/100mL
- 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 |
|---|
| 56152-4002-1 | Dark Spot Lightening Cream | 50 mL in 1 BOTTLE | CREAM | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56152-4002 | DARK SPOT LIGHTENING CREAM (HYDROQUINONE) CREAM [COSMETIC ENTERPRISES LTD.] | 1 | Legacy NDC, 1 package rows | 20190117_7d8d68c1-a16b-29d3-e053-2991aa0a0563.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 56152-4002-1 | 56152400201 | 50 mL in 1 BOTTLE | 50 ml | Historical |