| Product NDC: | 59779-830 | 
| Proprietary Name: | Mouth Sore Relief | 
| Non Proprietary Name: | Benzocaine | 
| Active Ingredient(s): | 200 mg/g & nbsp; Benzocaine | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-830 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part333B | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20091001 | 
| Package NDC: | 59779-830-38 | 
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 BLISTER PACK (59779-830-38) > 14.7 g in 1 BOTTLE, WITH APPLICATOR (59779-830-31) | 
| NDC Code | 59779-830-38 | 
| Proprietary Name | Mouth Sore Relief | 
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 BLISTER PACK (59779-830-38) > 14.7 g in 1 BOTTLE, WITH APPLICATOR (59779-830-31) | 
| Product NDC | 59779-830 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Benzocaine | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20091001 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | BENZOCAINE | 
| Strength Number | 200 | 
| Strength Unit | mg/g | 
| Pharmaceutical Classes |