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Genuine Triple Antibiotic
Genuine Triple Antibiotic - 52124-0003-1 - (BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE)
Drug Information of Genuine Triple Antibiotic
| Product NDC: | 52124-0003 |
| Proprietary Name: | Genuine Triple Antibiotic |
| Non Proprietary Name: | BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE |
| Active Ingredient(s): | 400; 5; 5000 [iU]/g; mg/g; [iU]/g & nbsp; BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Genuine Triple Antibiotic
| Product NDC: | 52124-0003 |
| Labeler Name: | Genuine First Aid LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100216 |
Package Information of Genuine Triple Antibiotic
| Package NDC: | 52124-0003-1 |
| Package Description: | .5 g in 1 TUBE (52124-0003-1) |
NDC Information of Genuine Triple Antibiotic
| NDC Code | 52124-0003-1 |
| Proprietary Name | Genuine Triple Antibiotic |
| Package Description | .5 g in 1 TUBE (52124-0003-1) |
| Product NDC | 52124-0003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100216 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Genuine First Aid LLC |
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 400; 5; 5000 |
| Strength Unit | [iU]/g; mg/g; [iU]/g |
| Pharmaceutical Classes |
