| Product NDC: | 63824-810 |
| Proprietary Name: | Lanacane |
| Non Proprietary Name: | Benzethonium chloride and Benzocaine |
| Active Ingredient(s): | 2; 200 mg/g; mg/g & nbsp; Benzethonium chloride and Benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63824-810 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120928 |
| Package NDC: | 63824-810-01 |
| Package Description: | 1 TUBE in 1 CARTON (63824-810-01) > 28 g in 1 TUBE |
| NDC Code | 63824-810-01 |
| Proprietary Name | Lanacane |
| Package Description | 1 TUBE in 1 CARTON (63824-810-01) > 28 g in 1 TUBE |
| Product NDC | 63824-810 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzethonium chloride and Benzocaine |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120928 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | BENZETHONIUM CHLORIDE; BENZOCAINE |
| Strength Number | 2; 200 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |