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Neosporin Original
Neosporin Original - 58232-4002-1 - (Bacitracin, Neomycin, and Polymyxin B)
Drug Information of Neosporin Original
| Product NDC: | 58232-4002 |
| Proprietary Name: | Neosporin Original |
| Non Proprietary Name: | Bacitracin, Neomycin, and Polymyxin B |
| Active Ingredient(s): | 400; 3.5; 5000 [iU]/g; mg/g; [iU]/g & nbsp; Bacitracin, Neomycin, and Polymyxin B |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neosporin Original
| Product NDC: | 58232-4002 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110803 |
Package Information of Neosporin Original
| Package NDC: | 58232-4002-1 |
| Package Description: | .9 g in 1 POUCH (58232-4002-1) |
NDC Information of Neosporin Original
| NDC Code | 58232-4002-1 |
| Proprietary Name | Neosporin Original |
| Package Description | .9 g in 1 POUCH (58232-4002-1) |
| Product NDC | 58232-4002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacitracin, Neomycin, and Polymyxin B |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110803 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | BACITRACIN; NEOMYCIN; POLYMYXIN B |
| Strength Number | 400; 3.5; 5000 |
| Strength Unit | [iU]/g; mg/g; [iU]/g |
| Pharmaceutical Classes |
