Product NDC: | 67777-217 |
Proprietary Name: | bacitracin zinc, neomycin sulfate and polymyxin b sulfate |
Non Proprietary Name: | bacitracin zinc, neomycin sulfate and polymyxin b sulfate |
Active Ingredient(s): | 400; 5; 5000 [iU]/g; mg/g; [iU]/g & nbsp; bacitracin zinc, neomycin sulfate and polymyxin b sulfate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67777-217 |
Labeler Name: | Dynarex Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091201 |
Package NDC: | 67777-217-03 |
Package Description: | 72 TUBE in 1 CASE (67777-217-03) > 56.7 g in 1 TUBE |
NDC Code | 67777-217-03 |
Proprietary Name | bacitracin zinc, neomycin sulfate and polymyxin b sulfate |
Package Description | 72 TUBE in 1 CASE (67777-217-03) > 56.7 g in 1 TUBE |
Product NDC | 67777-217 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | bacitracin zinc, neomycin sulfate and polymyxin b sulfate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20091201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dynarex Corporation |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
Strength Number | 400; 5; 5000 |
Strength Unit | [iU]/g; mg/g; [iU]/g |
Pharmaceutical Classes |