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sunmark - 49348-690-69 - (Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride)
Drug Information of sunmark
| Product NDC: | 49348-690 |
| Proprietary Name: | sunmark |
| 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 sunmark
| Product NDC: | 49348-690 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120321 |
Package Information of sunmark
| Package NDC: | 49348-690-69 |
| Package Description: | 1 TUBE in 1 CARTON (49348-690-69) > 14.2 g in 1 TUBE |
NDC Information of sunmark
| NDC Code | 49348-690-69 |
| Proprietary Name | sunmark |
| Package Description | 1 TUBE in 1 CARTON (49348-690-69) > 14.2 g in 1 TUBE |
| Product NDC | 49348-690 |
| 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 | 20120321 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| 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 |
