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Severe Oral Pain Reliever - 59779-820-31 - (Benzocaine)

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Drug Information of Severe Oral Pain Reliever

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)

Labeler Information of Severe Oral Pain Reliever

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 Information of Severe Oral Pain Reliever

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 Information of Severe Oral Pain Reliever

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

Complete Information of Severe Oral Pain Reliever


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