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Nioxin Scalp Recovery
Nioxin Scalp Recovery - 37000-739-20 - (Pyrithione Zinc)
Drug Information of Nioxin Scalp Recovery
| Product NDC: | 37000-739 |
| Proprietary Name: | Nioxin Scalp Recovery |
| Non Proprietary Name: | Pyrithione Zinc |
| Active Ingredient(s): | 1 mg/mL & nbsp; Pyrithione Zinc |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION/SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nioxin Scalp Recovery
| Product NDC: | 37000-739 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110101 |
Package Information of Nioxin Scalp Recovery
| Package NDC: | 37000-739-20 |
| Package Description: | 200 mL in 1 BOTTLE, PLASTIC (37000-739-20) |
NDC Information of Nioxin Scalp Recovery
| NDC Code | 37000-739-20 |
| Proprietary Name | Nioxin Scalp Recovery |
| Package Description | 200 mL in 1 BOTTLE, PLASTIC (37000-739-20) |
| Product NDC | 37000-739 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pyrithione Zinc |
| Dosage Form Name | LOTION/SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20110101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | PYRITHIONE ZINC |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
