Product NDC: | 63777-082 |
Proprietary Name: | Antibiotic and Pain Relief |
Non Proprietary Name: | bacitracin zinc neomycin sulfate polymyxin b sulfate pramoxine hcl |
Active Ingredient(s): | 500; 3.5; 10000; 10 [USP'U]/g; mg/g; [USP'U]/g; mg/g & nbsp; bacitracin zinc neomycin sulfate polymyxin b sulfate pramoxine hcl |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63777-082 |
Labeler Name: | Kinray, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100701 |
Package NDC: | 63777-082-31 |
Package Description: | 1 TUBE in 1 CARTON (63777-082-31) > 28 g in 1 TUBE |
NDC Code | 63777-082-31 |
Proprietary Name | Antibiotic and Pain Relief |
Package Description | 1 TUBE in 1 CARTON (63777-082-31) > 28 g in 1 TUBE |
Product NDC | 63777-082 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | bacitracin zinc neomycin sulfate polymyxin b sulfate pramoxine hcl |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kinray, Inc. |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE |
Strength Number | 500; 3.5; 10000; 10 |
Strength Unit | [USP'U]/g; mg/g; [USP'U]/g; mg/g |
Pharmaceutical Classes |