| Product NDC: | 37808-679 | 
| Proprietary Name: | triple antibiotic plus | 
| Non Proprietary Name: | Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl | 
| Active Ingredient(s): | 500; 3.5; 10000; 10 [USP'U]/g; mg/g; [USP'U]/g; mg/g & nbsp; Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | OINTMENT | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 37808-679 | 
| Labeler Name: | H E B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part333B | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20101105 | 
| Package NDC: | 37808-679-64 | 
| Package Description: | 1 TUBE in 1 CARTON (37808-679-64) > 28 g in 1 TUBE | 
| NDC Code | 37808-679-64 | 
| Proprietary Name | triple antibiotic plus | 
| Package Description | 1 TUBE in 1 CARTON (37808-679-64) > 28 g in 1 TUBE | 
| Product NDC | 37808-679 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl | 
| Dosage Form Name | OINTMENT | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20101105 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H E B | 
| 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 |