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 |