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Mouth Sore Relief - 59779-830-38 - (Benzocaine)

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Drug Information of Mouth Sore Relief

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)

Labeler Information of Mouth Sore Relief

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 Information of Mouth Sore Relief

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 Information of Mouth Sore Relief

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

Complete Information of Mouth Sore Relief


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