| 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 |