Home NDC 59779-123 CVS
Product NDC 59779-123
11-digit product format 597790123
Labeler code 59779
Product ID 59779-123_47e5d814-8498-9446-e063-6294a90afe14
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form PASTE, DENTIFRICE
Route TOPICAL
Labeler CVS Pharmacy
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-01-20
Substance BENZOCAINE
Active strength 20 g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 59779-123 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 59779-123 59779-123-19 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 CVS
Brand name suffix Maximum Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 g/100g
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 562785 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59779-123-19 CVSMaximum Strength 12 g in 1 TUBE PASTE, DENTIFRICE 12 14 59779-123-19 CVSMaximum Strength 1 in 1 CARTON PASTE, DENTIFRICE 1 14
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BENZOCAINE ACTIVE INGREDIENT U3RSY48JW5 CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 BENZOCAINE ACTIVE MOIETY U3RSY48JW5 CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 GELATIN INACTIVE INGREDIENT 2G86QN327L CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 MENTHOL INACTIVE INGREDIENT L7T10EIP3A CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 METHYL SALICYLATE INACTIVE INGREDIENT LAV5U5022Y CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 PECTIN INACTIVE INGREDIENT 89NA02M4RX CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 POLYETHYLENE GLYCOL 1000 INACTIVE INGREDIENT U076Q6Q621 CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3 SACCHARIN INACTIVE INGREDIENT FST467XS7D CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59779-123 CVS MAXIMUM STRENGTH (BENZOCAINE) PASTE, DENTIFRICE [CVS PHARMACY] 13 Current NDC, Legacy NDC, 2 package rows 20250121_8691d6b6-741e-47b2-8332-76742b34715f.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 9 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 59779-123-19 59779012319 1 TUBE in 1 CARTON (59779-123-19) / 12 g in 1 TUBE 1 tube 2011-01-20 0000-00-00 No No Current