Product NDC: | 0924-5603 |
Proprietary Name: | triple antibiotic |
Non Proprietary Name: | bacitracin zinc, neomycin sulfate, polymyxin b sulfate |
Active Ingredient(s): | 400; 3.5; 5000 [iU]/g; mg/g; [iU]/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: | 0924-5603 |
Labeler Name: | Acme United Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120127 |
Package NDC: | 0924-5603-07 |
Package Description: | 144 PACKET in 1 BOX (0924-5603-07) > .5 g in 1 PACKET (0924-5603-01) (0924-5603-01) |
NDC Code | 0924-5603-07 |
Proprietary Name | triple antibiotic |
Package Description | 144 PACKET in 1 BOX (0924-5603-07) > .5 g in 1 PACKET (0924-5603-01) (0924-5603-01) |
Product NDC | 0924-5603 |
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 | 20120127 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Acme United Corporation |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
Strength Number | 400; 3.5; 5000 |
Strength Unit | [iU]/g; mg/g; [iU]/g |
Pharmaceutical Classes |