Product NDC: | 55301-823 |
Proprietary Name: | Triple Antibiotic Plus |
Non Proprietary Name: | bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl |
Active Ingredient(s): | 500; 3.5; 10000; 10 [USP'U]/g; mg/g; [USP'U]/g; mg/g & nbsp; bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55301-823 |
Labeler Name: | Exchange Select |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20050301 |
Package NDC: | 55301-823-56 |
Package Description: | 1 TUBE in 1 CARTON (55301-823-56) > 28 g in 1 TUBE |
NDC Code | 55301-823-56 |
Proprietary Name | Triple Antibiotic Plus |
Package Description | 1 TUBE in 1 CARTON (55301-823-56) > 28 g in 1 TUBE |
Product NDC | 55301-823 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20050301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Exchange Select |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE |
Strength Number | 500; 3.5; 10000; 10 |
Strength Unit | [USP'U]/g; mg/g; [USP'U]/g; mg/g |
Pharmaceutical Classes |