| Product NDC: | 50607-5600 |
| Proprietary Name: | Triple Antibiotic |
| Non Proprietary Name: | Triple Antibiotic |
| Active Ingredient(s): | 400; 5; 5000 1/g; mg/g; 1/g & nbsp; Triple Antibiotic |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50607-5600 |
| Labeler Name: | B8 Sales, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100501 |
| Package NDC: | 50607-5600-2 |
| Package Description: | 144 POUCH in 1 BOX (50607-5600-2) > .9 g in 1 POUCH |
| NDC Code | 50607-5600-2 |
| Proprietary Name | Triple Antibiotic |
| Package Description | 144 POUCH in 1 BOX (50607-5600-2) > .9 g in 1 POUCH |
| Product NDC | 50607-5600 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triple Antibiotic |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | B8 Sales, Inc. |
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 400; 5; 5000 |
| Strength Unit | 1/g; mg/g; 1/g |
| Pharmaceutical Classes |