| Product NDC: | 11509-0306 |
| Proprietary Name: | Lanacane Anti Itch Maximum Strength |
| Non Proprietary Name: | benzocaine and benzethonium chloride |
| Active Ingredient(s): | 2; 200 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: | 11509-0306 |
| 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: | 11509-0306-1 |
| Package Description: | 1 TUBE in 1 CARTON (11509-0306-1) > 28 g in 1 TUBE |
| NDC Code | 11509-0306-1 |
| Proprietary Name | Lanacane Anti Itch Maximum Strength |
| Package Description | 1 TUBE in 1 CARTON (11509-0306-1) > 28 g in 1 TUBE |
| Product NDC | 11509-0306 |
| 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; 200 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |