Product NDC: | 11509-0301 |
Proprietary Name: | Lanacane Anti Itch Original Strength |
Non Proprietary Name: | benzocaine and benzethonium chloride |
Active Ingredient(s): | 2; 60 mg/g; mg/g & nbsp; benzocaine and benzethonium chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11509-0301 |
Labeler Name: | Combe Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19971231 |
Package NDC: | 11509-0301-1 |
Package Description: | 1 TUBE in 1 CARTON (11509-0301-1) > 28 g in 1 TUBE |
NDC Code | 11509-0301-1 |
Proprietary Name | Lanacane Anti Itch Original Strength |
Package Description | 1 TUBE in 1 CARTON (11509-0301-1) > 28 g in 1 TUBE |
Product NDC | 11509-0301 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | benzocaine and benzethonium chloride |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19971231 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Combe Incorporated |
Substance Name | BENZETHONIUM CHLORIDE; BENZOCAINE |
Strength Number | 2; 60 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |