SELENIUM SULFIDE
- Product NDC
- 68071-1768
- 11-digit product format
- 680711768
- Labeler code
- 68071
- Product ID
- 68071-1768_c46d2f34-29cb-11fc-e053-2a95a90a84ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SELENIUM SULFIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- NuCare 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Z69D9E381Q | SELENIUM SULFIDE | 7488-56-4 | SELENIUM SULFIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1768-4 | 68071176804 | 118 mL in 1 BOTTLE (68071-1768-4) | 118 ml | 2021-06-10 | 0000-00-00 | No | No | Current |