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 |