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Pantene Pro-V
Pantene Pro-V - 37000-051-75 - (pyrithione zinc)
Drug Information of Pantene Pro-V
| Product NDC: | 37000-051 |
| Proprietary Name: | Pantene Pro-V |
| Non Proprietary Name: | pyrithione zinc |
| Active Ingredient(s): | 1 g/mL & nbsp; pyrithione zinc |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION/SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pantene Pro-V
| Product NDC: | 37000-051 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120201 |
Package Information of Pantene Pro-V
| Package NDC: | 37000-051-75 |
| Package Description: | 750 mL in 1 BOTTLE, PLASTIC (37000-051-75) |
NDC Information of Pantene Pro-V
| NDC Code | 37000-051-75 |
| Proprietary Name | Pantene Pro-V |
| Package Description | 750 mL in 1 BOTTLE, PLASTIC (37000-051-75) |
| Product NDC | 37000-051 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | pyrithione zinc |
| Dosage Form Name | LOTION/SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | PYRITHIONE ZINC |
| Strength Number | 1 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
