Home NDC 59779-830 Mouth Sore Relief
Product NDC 59779-830
11-digit product format 597790830
Labeler code 59779
Product ID 59779-830_4005a1a1-f3aa-bd0f-e063-6394a90a1a61
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form LIQUID
Route ORAL
Labeler CVS Pharmacy
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2009-10-01
Substance BENZOCAINE
Active strength 200 mg/g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Mouth Sore Relief
Brand name suffix Professional Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308657 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59779-830-38 Mouth Sore ReliefProfessional Strength 1 in 1 BLISTER PACK LIQUID 1 24 59779-830-38 Mouth Sore ReliefProfessional Strength 14.7 g in 1 BOTTLE, WITH APPLICATOR LIQUID 14.7 24 59779-830-48 Mouth Sore ReliefProfessional Strength 1 in 1 BLISTER PACK LIQUID 1 24 59779-830-48 Mouth Sore ReliefProfessional Strength 14.7 g in 1 BOTTLE LIQUID 14.7 24
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59779-830 MOUTH SORE RELIEF PROFESSIONAL STRENGTH (BENZOCAINE) LIQUID [CVS PHARMACY] 22 Current NDC, Legacy NDC, 4 package rows 20250119_1b7209f6-8368-47fa-8df2-b049613b8c1b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 14 of 40 · 786 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59779-830-38 59779083038 1 BOTTLE, WITH APPLICATOR in 1 BLISTER PACK (59779-830-38) / 14.7 g in 1 BOTTLE, WITH APPLICATOR 2011-04-19 0000-00-00 No No Current 59779-830-48 59779083048 1 BOTTLE in 1 BLISTER PACK (59779-830-48) / 14.7 g in 1 BOTTLE 1 bottle 2011-04-19 0000-00-00 No No Current