| Product NDC: | 55154-1953 |
| Proprietary Name: | Triple Antibiotic |
| Non Proprietary Name: | Polymyxin B, Bacitracin, Neomycin |
| Active Ingredient(s): | 400; 3.5; 5000 [USP'U]/1; mg/1; [USP'U]/1 & nbsp; Polymyxin B, Bacitracin, Neomycin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-1953 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110606 |
| Package NDC: | 55154-1953-8 |
| Package Description: | 1 PACKET in 1 BAG (55154-1953-8) > 1 OINTMENT in 1 PACKET |
| NDC Code | 55154-1953-8 |
| Proprietary Name | Triple Antibiotic |
| Package Description | 1 PACKET in 1 BAG (55154-1953-8) > 1 OINTMENT in 1 PACKET |
| Product NDC | 55154-1953 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polymyxin B, Bacitracin, Neomycin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110606 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | BACITRACIN; NEOMYCIN SULFATE; POLYMYXIN B |
| Strength Number | 400; 3.5; 5000 |
| Strength Unit | [USP'U]/1; mg/1; [USP'U]/1 |
| Pharmaceutical Classes |