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Nioxin Scalp Shield Sunscreen
Nioxin Scalp Shield Sunscreen - 37000-734-10 - (ensulizole and sulisobenzone)
Drug Information of Nioxin Scalp Shield Sunscreen
| Product NDC: | 37000-734 |
| Proprietary Name: | Nioxin Scalp Shield Sunscreen |
| Non Proprietary Name: | ensulizole and sulisobenzone |
| Active Ingredient(s): | 40; 25 mg/mL; mg/mL & nbsp; ensulizole and sulisobenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nioxin Scalp Shield Sunscreen
| Product NDC: | 37000-734 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110101 |
Package Information of Nioxin Scalp Shield Sunscreen
| Package NDC: | 37000-734-10 |
| Package Description: | 100 mL in 1 BOTTLE, SPRAY (37000-734-10) |
NDC Information of Nioxin Scalp Shield Sunscreen
| NDC Code | 37000-734-10 |
| Proprietary Name | Nioxin Scalp Shield Sunscreen |
| Package Description | 100 mL in 1 BOTTLE, SPRAY (37000-734-10) |
| Product NDC | 37000-734 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ensulizole and sulisobenzone |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | ENSULIZOLE; SULISOBENZONE |
| Strength Number | 40; 25 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
