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Neosporin Original
Neosporin Original - 58232-0423-1 - (Bacitracin, Neomycin, Polymyxin B)
Drug Information of Neosporin Original
| Product NDC: | 58232-0423 |
| Proprietary Name: | Neosporin Original |
| Non Proprietary Name: | Bacitracin, Neomycin, Polymyxin B |
| Active Ingredient(s): | & nbsp; Bacitracin, Neomycin, Polymyxin B |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neosporin Original
| Product NDC: | 58232-0423 |
| 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: | 20110804 |
Package Information of Neosporin Original
| Package NDC: | 58232-0423-1 |
| Package Description: | 1 KIT in 1 BLISTER PACK (58232-0423-1) * 2 TUBE in 1 CARTON > 14.2 g in 1 TUBE * 1 TUBE in 1 CARTON > 28.3 g in 1 TUBE |
NDC Information of Neosporin Original
| NDC Code | 58232-0423-1 |
| Proprietary Name | Neosporin Original |
| Package Description | 1 KIT in 1 BLISTER PACK (58232-0423-1) * 2 TUBE in 1 CARTON > 14.2 g in 1 TUBE * 1 TUBE in 1 CARTON > 28.3 g in 1 TUBE |
| Product NDC | 58232-0423 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacitracin, Neomycin, Polymyxin B |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110804 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
