| 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 |