SELENIUM SULFIDE
- Product NDC
- 53002-8260
- 11-digit product format
- 530028260
- Labeler code
- 53002
- Product ID
- 53002-8260_fd1af4fd-cc56-4732-85de-647646634e91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SELENIUM SULFIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA089996
- Marketing category
- ANDA
- Marketing start
- 2006-09-25
- Marketing end
- 0000-00-00
- Substance
- SELENIUM SULFIDE
- Active strength
- 3 mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53002-8260-1 | SELENIUM SULFIDE | 118 mL in 1 BOTTLE | LOTION | 118 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-8260 | SELENIUM SULFIDE LOTION [RPK PHARMACEUTICALS, INC.] | 5 | Legacy NDC, 1 package rows | 20230609_4c656fee-544a-4279-b77f-ecb77cf6f0c4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-8260-1 | 53002826001 | 118 mL in 1 BOTTLE (53002-8260-1) | 118 ml | 2018-10-01 | 0000-00-00 | No | No | Current |