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Polysporin
Polysporin - 58232-4033-1 - (Polymyxin B Sulfate and Bacitracin Zinc)
Drug Information of Polysporin
| Product NDC: | 58232-4033 |
| Proprietary Name: | Polysporin |
| Non Proprietary Name: | Polymyxin B Sulfate and Bacitracin Zinc |
| Active Ingredient(s): | 500; 10000 [USP'U]/g; [USP'U]/g & nbsp; Polymyxin B Sulfate and Bacitracin Zinc |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Polysporin
| Product NDC: | 58232-4033 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100614 |
Package Information of Polysporin
| Package NDC: | 58232-4033-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (58232-4033-1) > 10 g in 1 BOTTLE |
NDC Information of Polysporin
| NDC Code | 58232-4033-1 |
| Proprietary Name | Polysporin |
| Package Description | 1 BOTTLE in 1 CARTON (58232-4033-1) > 10 g in 1 BOTTLE |
| Product NDC | 58232-4033 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polymyxin B Sulfate and Bacitracin Zinc |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20100614 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | BACITRACIN ZINC; POLYMYXIN B SULFATE |
| Strength Number | 500; 10000 |
| Strength Unit | [USP'U]/g; [USP'U]/g |
| Pharmaceutical Classes |
