Product NDC: | 53329-087 |
Proprietary Name: | Triple Antibiotic |
Non Proprietary Name: | bacitracin zinc, neomycin sulfate, polymyxin B sulfate |
Active Ingredient(s): | 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g & nbsp; bacitracin zinc, neomycin sulfate, polymyxin B sulfate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53329-087 |
Labeler Name: | Medline Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100401 |
Package NDC: | 53329-087-96 |
Package Description: | 144 PACKET in 1 BOX (53329-087-96) > .9 g in 1 PACKET (53329-087-87) |
NDC Code | 53329-087-96 |
Proprietary Name | Triple Antibiotic |
Package Description | 144 PACKET in 1 BOX (53329-087-96) > .9 g in 1 PACKET (53329-087-87) |
Product NDC | 53329-087 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | bacitracin zinc, neomycin sulfate, polymyxin B sulfate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Medline Industries, Inc. |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
Strength Number | 400; 3.5; 5000 |
Strength Unit | [USP'U]/g; mg/g; [USP'U]/g |
Pharmaceutical Classes |