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ANTIDANDRUFF
ANTIDANDRUFF - 59779-610-11 - (SELENIUM SULFIDE)
Drug Information of ANTIDANDRUFF
| Product NDC: | 59779-610 |
| Proprietary Name: | ANTIDANDRUFF |
| 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) |
Labeler Information of ANTIDANDRUFF
| Product NDC: | 59779-610 |
| Labeler Name: | CVS PHARMACY INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100706 |
Package Information of ANTIDANDRUFF
| Package NDC: | 59779-610-11 |
| Package Description: | 325 mL in 1 BOTTLE, PLASTIC (59779-610-11) |
NDC Information of ANTIDANDRUFF
| NDC Code | 59779-610-11 |
| Proprietary Name | ANTIDANDRUFF |
| Package Description | 325 mL in 1 BOTTLE, PLASTIC (59779-610-11) |
| Product NDC | 59779-610 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SELENIUM SULFIDE |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20100706 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS PHARMACY INC |
| Substance Name | SELENIUM SULFIDE |
| Strength Number | 1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
