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Dandruff
Dandruff - 36800-309-15 - (Pyrithione Zinc)
Drug Information of Dandruff
| Product NDC: | 36800-309 |
| Proprietary Name: | Dandruff |
| Non Proprietary Name: | Pyrithione Zinc |
| Active Ingredient(s): | 1 g/100mL & nbsp; Pyrithione Zinc |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dandruff
| Product NDC: | 36800-309 |
| Labeler Name: | Topco Associates |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110210 |
Package Information of Dandruff
| Package NDC: | 36800-309-15 |
| Package Description: | 420 mL in 1 BOTTLE, PLASTIC (36800-309-15) |
NDC Information of Dandruff
| NDC Code | 36800-309-15 |
| Proprietary Name | Dandruff |
| Package Description | 420 mL in 1 BOTTLE, PLASTIC (36800-309-15) |
| Product NDC | 36800-309 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pyrithione Zinc |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20110210 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Topco Associates |
| Substance Name | PYRITHIONE ZINC |
| Strength Number | 1 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
