Product NDC: | 52124-0003 |
Proprietary Name: | Genuine Triple Antibiotic |
Non Proprietary Name: | BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE |
Active Ingredient(s): | 400; 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: | 52124-0003 |
Labeler Name: | Genuine First Aid LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100216 |
Package NDC: | 52124-0003-2 |
Package Description: | 10 PACKET in 1 BOX (52124-0003-2) > .5 g in 1 PACKET |
NDC Code | 52124-0003-2 |
Proprietary Name | Genuine Triple Antibiotic |
Package Description | 10 PACKET in 1 BOX (52124-0003-2) > .5 g in 1 PACKET |
Product NDC | 52124-0003 |
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 | 20100216 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Genuine First Aid LLC |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
Strength Number | 400; 5; 5000 |
Strength Unit | [iU]/g; mg/g; [iU]/g |
Pharmaceutical Classes |