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Zincon Medicated Dandruff
Zincon Medicated Dandruff - 51545-250-08 - (Pyrithione zinc)
Drug Information of Zincon Medicated Dandruff
| Product NDC: | 51545-250 |
| Proprietary Name: | Zincon Medicated Dandruff |
| Non Proprietary Name: | Pyrithione zinc |
| Active Ingredient(s): | .01 g/mL & nbsp; Pyrithione zinc |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zincon Medicated Dandruff
| Product NDC: | 51545-250 |
| Labeler Name: | Ultimark Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101101 |
Package Information of Zincon Medicated Dandruff
| Package NDC: | 51545-250-08 |
| Package Description: | 118 mL in 1 BOTTLE (51545-250-08) |
NDC Information of Zincon Medicated Dandruff
| NDC Code | 51545-250-08 |
| Proprietary Name | Zincon Medicated Dandruff |
| Package Description | 118 mL in 1 BOTTLE (51545-250-08) |
| Product NDC | 51545-250 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pyrithione zinc |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20101101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultimark Products LLC |
| Substance Name | PYRITHIONE ZINC |
| Strength Number | .01 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
