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Dandruff
Dandruff - 41520-311-15 - (Pyrithione zinc)
Drug Information of Dandruff
| Product NDC: | 41520-311 |
| Proprietary Name: | Dandruff |
| Non Proprietary Name: | Pyrithione zinc |
| Active Ingredient(s): | 1 g/100mL & nbsp; Pyrithione zinc |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION/SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dandruff
| Product NDC: | 41520-311 |
| Labeler Name: | American Sales Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040709 |
Package Information of Dandruff
| Package NDC: | 41520-311-15 |
| Package Description: | 420 mL in 1 BOTTLE, PLASTIC (41520-311-15) |
NDC Information of Dandruff
| NDC Code | 41520-311-15 |
| Proprietary Name | Dandruff |
| Package Description | 420 mL in 1 BOTTLE, PLASTIC (41520-311-15) |
| Product NDC | 41520-311 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pyrithione zinc |
| Dosage Form Name | LOTION/SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20040709 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | American Sales Company |
| Substance Name | PYRITHIONE ZINC |
| Strength Number | 1 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
