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ANTIBIOTIC PLUS PAIN RELIEF
ANTIBIOTIC PLUS PAIN RELIEF - 52426-220-05 - (Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride)
Drug Information of ANTIBIOTIC PLUS PAIN RELIEF
| Product NDC: | 52426-220 |
| Proprietary Name: | ANTIBIOTIC PLUS PAIN RELIEF |
| Non Proprietary Name: | Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride |
| Active Ingredient(s): | 3.5; 10000; 10 mg/g; [iU]/g; mg/g & nbsp; Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ANTIBIOTIC PLUS PAIN RELIEF
| Product NDC: | 52426-220 |
| Labeler Name: | Phoenix Global Supply Group, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110701 |
Package Information of ANTIBIOTIC PLUS PAIN RELIEF
| Package NDC: | 52426-220-05 |
| Package Description: | 1 TUBE in 1 CARTON (52426-220-05) > 14.2 g in 1 TUBE |
NDC Information of ANTIBIOTIC PLUS PAIN RELIEF
| NDC Code | 52426-220-05 |
| Proprietary Name | ANTIBIOTIC PLUS PAIN RELIEF |
| Package Description | 1 TUBE in 1 CARTON (52426-220-05) > 14.2 g in 1 TUBE |
| Product NDC | 52426-220 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Phoenix Global Supply Group, Inc. |
| Substance Name | NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 3.5; 10000; 10 |
| Strength Unit | mg/g; [iU]/g; mg/g |
| Pharmaceutical Classes |
