| Product NDC: | 43596-0021 |
| Proprietary Name: | Esika Men Dandruff |
| Non Proprietary Name: | PYRITHIONE ZINC |
| Active Ingredient(s): | 5.28 mg/mL & nbsp; PYRITHIONE ZINC |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43596-0021 |
| Labeler Name: | Ventura Corporation Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121003 |
| Package NDC: | 43596-0021-0 |
| Package Description: | 5 mL in 1 PACKET (43596-0021-0) |
| NDC Code | 43596-0021-0 |
| Proprietary Name | Esika Men Dandruff |
| Package Description | 5 mL in 1 PACKET (43596-0021-0) |
| Product NDC | 43596-0021 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PYRITHIONE ZINC |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20121003 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura Corporation Limited |
| Substance Name | PYRITHIONE ZINC |
| Strength Number | 5.28 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |