| Product NDC: | 54569-1139 |
| Proprietary Name: | SELENIUM SULFIDE |
| Non Proprietary Name: | SELENIUM SULFIDE |
| Active Ingredient(s): | 2.5 mg/100mL & nbsp; SELENIUM SULFIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54569-1139 |
| Labeler Name: | A-S Medication Solutions LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089996 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060925 |
| Package NDC: | 54569-1139-0 |
| Package Description: | 120 mL in 1 BOTTLE (54569-1139-0) |
| NDC Code | 54569-1139-0 |
| Proprietary Name | SELENIUM SULFIDE |
| Package Description | 120 mL in 1 BOTTLE (54569-1139-0) |
| Product NDC | 54569-1139 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SELENIUM SULFIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060925 |
| Marketing Category Name | ANDA |
| Labeler Name | A-S Medication Solutions LLC |
| Substance Name | SELENIUM SULFIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |