| Product NDC: | 59779-820 | 
| Proprietary Name: | Severe Oral Pain Reliever | 
| Non Proprietary Name: | Benzocaine | 
| Active Ingredient(s): | 20 g/100g & nbsp; Benzocaine | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-820 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part333B | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20111227 | 
| Package NDC: | 59779-820-31 | 
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (59779-820-31) > 14.17 g in 1 BOTTLE, WITH APPLICATOR (59779-820-39) | 
| NDC Code | 59779-820-31 | 
| Proprietary Name | Severe Oral Pain Reliever | 
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (59779-820-31) > 14.17 g in 1 BOTTLE, WITH APPLICATOR (59779-820-39) | 
| Product NDC | 59779-820 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Benzocaine | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20111227 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | BENZOCAINE | 
| Strength Number | 20 | 
| Strength Unit | g/100g | 
| Pharmaceutical Classes |