Product NDC: | 41520-614 |
Proprietary Name: | MEDICATED DANDRUFF |
Non Proprietary Name: | SELENIUM SULFIDE |
Active Ingredient(s): | 1 mL/100mL & nbsp; SELENIUM SULFIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SHAMPOO |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41520-614 |
Labeler Name: | AMERICAN SALES COMPANY |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358H |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110819 |
Package NDC: | 41520-614-11 |
Package Description: | 325 mL in 1 BOTTLE (41520-614-11) |
NDC Code | 41520-614-11 |
Proprietary Name | MEDICATED DANDRUFF |
Package Description | 325 mL in 1 BOTTLE (41520-614-11) |
Product NDC | 41520-614 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SELENIUM SULFIDE |
Dosage Form Name | SHAMPOO |
Route Name | TOPICAL |
Start Marketing Date | 20110819 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | AMERICAN SALES COMPANY |
Substance Name | SELENIUM SULFIDE |
Strength Number | 1 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |