Product NDC: | 63868-945 |
Proprietary Name: | QUALITY CHOICE TRIPLE ANTIBIOTIC PLUS PAIN RELIEVER |
Non Proprietary Name: | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, PRAMOXINE HYDROCHLORIDE |
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 HYDROCHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63868-945 |
Labeler Name: | CHAIN DRUG MARKETING ASSOCIATION INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120209 |
Package NDC: | 63868-945-94 |
Package Description: | 1 TUBE in 1 CARTON (63868-945-94) > 28 g in 1 TUBE |
NDC Code | 63868-945-94 |
Proprietary Name | QUALITY CHOICE TRIPLE ANTIBIOTIC PLUS PAIN RELIEVER |
Package Description | 1 TUBE in 1 CARTON (63868-945-94) > 28 g in 1 TUBE |
Product NDC | 63868-945 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, PRAMOXINE HYDROCHLORIDE |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20120209 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CHAIN DRUG MARKETING ASSOCIATION 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 |