Product NDC: | 54569-1111 |
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: | 54569-1111 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110601 |
Package NDC: | 54569-1111-0 |
Package Description: | 30 g in 1 TUBE (54569-1111-0) |
NDC Code | 54569-1111-0 |
Proprietary Name | TRIPLE ANTIBIOTIC |
Package Description | 30 g in 1 TUBE (54569-1111-0) |
Product NDC | 54569-1111 |
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 | 20110601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | A-S Medication Solutions LLC |
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 |