Product NDC: | 50607-5600 |
Proprietary Name: | Triple Antibiotic |
Non Proprietary Name: | Triple Antibiotic |
Active Ingredient(s): | 400; 5; 5000 1/g; mg/g; 1/g & nbsp; Triple Antibiotic |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50607-5600 |
Labeler Name: | B8 Sales, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100501 |
Package NDC: | 50607-5600-2 |
Package Description: | 144 POUCH in 1 BOX (50607-5600-2) > .9 g in 1 POUCH |
NDC Code | 50607-5600-2 |
Proprietary Name | Triple Antibiotic |
Package Description | 144 POUCH in 1 BOX (50607-5600-2) > .9 g in 1 POUCH |
Product NDC | 50607-5600 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Triple Antibiotic |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100501 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | B8 Sales, Inc. |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
Strength Number | 400; 5; 5000 |
Strength Unit | 1/g; mg/g; 1/g |
Pharmaceutical Classes |