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Dandruff
Dandruff - 59779-589-15 - (Selenium sulfide)
Drug Information of Dandruff
| Product NDC: | 59779-589 |
| Proprietary Name: | Dandruff |
| Non Proprietary Name: | Selenium sulfide |
| Active Ingredient(s): | 10 mg/mL & nbsp; Selenium sulfide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dandruff
| Product NDC: | 59779-589 |
| Labeler Name: | CVS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121209 |
Package Information of Dandruff
| Package NDC: | 59779-589-15 |
| Package Description: | 420 mL in 1 BOTTLE, PLASTIC (59779-589-15) |
NDC Information of Dandruff
| NDC Code | 59779-589-15 |
| Proprietary Name | Dandruff |
| Package Description | 420 mL in 1 BOTTLE, PLASTIC (59779-589-15) |
| Product NDC | 59779-589 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Selenium sulfide |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20121209 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS |
| Substance Name | SELENIUM SULFIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
