| Product NDC: | 0713-0268 |
| Proprietary Name: | Triple Antibiotic Ointment |
| Non Proprietary Name: | Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate |
| Active Ingredient(s): | 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g & nbsp; Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0713-0268 |
| Labeler Name: | G&W Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19950111 |
| Package NDC: | 0713-0268-31 |
| Package Description: | 28.4 g in 1 TUBE (0713-0268-31) |
| NDC Code | 0713-0268-31 |
| Proprietary Name | Triple Antibiotic Ointment |
| Package Description | 28.4 g in 1 TUBE (0713-0268-31) |
| Product NDC | 0713-0268 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19950111 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | G&W Laboratories, Inc. |
| Substance Name | BACITRACIN ZINC; NEOMYCIN; POLYMYXIN B SULFATE |
| Strength Number | 400; 3.5; 5000 |
| Strength Unit | [USP'U]/g; mg/g; [USP'U]/g |
| Pharmaceutical Classes |