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Triple Antibiotic Plus Pain Relief
Triple Antibiotic Plus Pain Relief - 51672-2027-2 - (Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride)
Drug Information of Triple Antibiotic Plus Pain Relief
| Product NDC: | 51672-2027 |
| Proprietary Name: | Triple Antibiotic Plus Pain Relief |
| Non Proprietary Name: | Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride |
| Active Ingredient(s): | 500; 3.5; 10000; 10 [USP'U]/g; mg/g; [USP'U]/g; mg/g & nbsp; Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Triple Antibiotic Plus Pain Relief
| Product NDC: | 51672-2027 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120331 |
Package Information of Triple Antibiotic Plus Pain Relief
| Package NDC: | 51672-2027-2 |
| Package Description: | 1 TUBE in 1 CARTON (51672-2027-2) > 28.4 g in 1 TUBE |
NDC Information of Triple Antibiotic Plus Pain Relief
| NDC Code | 51672-2027-2 |
| Proprietary Name | Triple Antibiotic Plus Pain Relief |
| Package Description | 1 TUBE in 1 CARTON (51672-2027-2) > 28.4 g in 1 TUBE |
| Product NDC | 51672-2027 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120331 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 500; 3.5; 10000; 10 |
| Strength Unit | [USP'U]/g; mg/g; [USP'U]/g; mg/g |
| Pharmaceutical Classes |
