Home
>
National Drug Code (NDC)
>
Neosporin Plus Pain Relief
Neosporin Plus Pain Relief - 58232-4013-8 - (Neomycin, Polymyxin B, and Pramoxine Hydrochloride)
Drug Information of Neosporin Plus Pain Relief
| Product NDC: | 58232-4013 |
| Proprietary Name: | Neosporin Plus Pain Relief |
| Non Proprietary Name: | Neomycin, Polymyxin B, and Pramoxine Hydrochloride |
| Active Ingredient(s): | 3.5; 10000; 10 mg/g; [USP'U]/g; mg/g & nbsp; Neomycin, Polymyxin B, and Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neosporin Plus Pain Relief
| Product NDC: | 58232-4013 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130627 |
Package Information of Neosporin Plus Pain Relief
| Package NDC: | 58232-4013-8 |
| Package Description: | 1 TUBE in 1 CARTON (58232-4013-8) > 18.4 g in 1 TUBE |
NDC Information of Neosporin Plus Pain Relief
| NDC Code | 58232-4013-8 |
| Proprietary Name | Neosporin Plus Pain Relief |
| Package Description | 1 TUBE in 1 CARTON (58232-4013-8) > 18.4 g in 1 TUBE |
| Product NDC | 58232-4013 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Neomycin, Polymyxin B, and Pramoxine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130627 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | NEOMYCIN; POLYMYXIN B; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 3.5; 10000; 10 |
| Strength Unit | mg/g; [USP'U]/g; mg/g |
| Pharmaceutical Classes |
