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Dandruff
Dandruff - 49348-890-71 - (Pyrithione zinc)
Drug Information of Dandruff
| Product NDC: | 49348-890 |
| Proprietary Name: | Dandruff |
| Non Proprietary Name: | Pyrithione zinc |
| Active Ingredient(s): | 1 kg/100L & nbsp; Pyrithione zinc |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dandruff
| Product NDC: | 49348-890 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20061206 |
Package Information of Dandruff
| Package NDC: | 49348-890-71 |
| Package Description: | .42 L in 1 BOTTLE, PLASTIC (49348-890-71) |
NDC Information of Dandruff
| NDC Code | 49348-890-71 |
| Proprietary Name | Dandruff |
| Package Description | .42 L in 1 BOTTLE, PLASTIC (49348-890-71) |
| Product NDC | 49348-890 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pyrithione zinc |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20061206 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | PYRITHIONE ZINC |
| Strength Number | 1 |
| Strength Unit | kg/100L |
| Pharmaceutical Classes |
