Product NDC: | 49348-600 |
Proprietary Name: | sunmark |
Non Proprietary Name: | polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride |
Active Ingredient(s): | 500; 3.5; 10000; 10 [iU]/g; mg/g; [iU]/g; mg/g & nbsp; polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-600 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120331 |
Package NDC: | 49348-600-72 |
Package Description: | 1 TUBE in 1 CARTON (49348-600-72) > 28.4 g in 1 TUBE |
NDC Code | 49348-600-72 |
Proprietary Name | sunmark |
Package Description | 1 TUBE in 1 CARTON (49348-600-72) > 28.4 g in 1 TUBE |
Product NDC | 49348-600 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20120331 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McKesson |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE |
Strength Number | 500; 3.5; 10000; 10 |
Strength Unit | [iU]/g; mg/g; [iU]/g; mg/g |
Pharmaceutical Classes |