Product NDC: | 11673-891 |
Proprietary Name: | up and up first aid antibiotic pain relieving |
Non Proprietary Name: | Neomycin, Polymyxin B, Pramoxine HCl |
Active Ingredient(s): | 3.5; 10000; 10 mg/g; [USP'U]/g; mg/g & nbsp; Neomycin, Polymyxin B, Pramoxine HCl |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11673-891 |
Labeler Name: | Target Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091117 |
Package NDC: | 11673-891-58 |
Package Description: | 1 TUBE in 1 CARTON (11673-891-58) > 14 g in 1 TUBE |
NDC Code | 11673-891-58 |
Proprietary Name | up and up first aid antibiotic pain relieving |
Package Description | 1 TUBE in 1 CARTON (11673-891-58) > 14 g in 1 TUBE |
Product NDC | 11673-891 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Neomycin, Polymyxin B, Pramoxine HCl |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20091117 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Target Corporation |
Substance Name | NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE |
Strength Number | 3.5; 10000; 10 |
Strength Unit | mg/g; [USP'U]/g; mg/g |
Pharmaceutical Classes |