Product NDC: | 52959-014 |
Proprietary Name: | Neomycin and Polymyxin B Sulfates and Bacitracin Zinc |
Non Proprietary Name: | Neomycin and Polymyxin B Sulfates and Bacitracin Zinc |
Active Ingredient(s): | 400; 5; 5000 [USP'U]/g; mg/g; [USP'U]/g & nbsp; Neomycin and Polymyxin B Sulfates and Bacitracin Zinc |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52959-014 |
Labeler Name: | H.J. Harkins Company, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100106 |
Package NDC: | 52959-014-03 |
Package Description: | 28.34 g in 1 TUBE (52959-014-03) |
NDC Code | 52959-014-03 |
Proprietary Name | Neomycin and Polymyxin B Sulfates and Bacitracin Zinc |
Package Description | 28.34 g in 1 TUBE (52959-014-03) |
Product NDC | 52959-014 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Neomycin and Polymyxin B Sulfates and Bacitracin Zinc |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100106 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | H.J. Harkins Company, Inc. |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
Strength Number | 400; 5; 5000 |
Strength Unit | [USP'U]/g; mg/g; [USP'U]/g |
Pharmaceutical Classes |