Home NDC 69842-353 Toothache and Gum Relief
Product NDC 69842-353
11-digit product format 698420353
Labeler code 69842
Product ID 69842-353_47e5f657-c064-b740-e063-6394a90a114e
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine, menthol
Dosage form LIQUID
Route TOPICAL
Labeler CVS Pharmacy
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-02-07
Substance BENZOCAINE; MENTHOL
Active strength 20; .1 g/100mL; g/100mL
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 69842-353 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 69842-353 69842-353-29 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 Toothache and Gum Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 g/100mL MENTHOL .1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2110600 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 69842-353-29 Toothache and Gum Relief 14.7 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 14.7 7 69842-353-29 Toothache and Gum Relief 1 in 1 CARTON LIQUID 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-353 TOOTHACHE AND GUM RELIEF (BENZOCAINE, MENTHOL) LIQUID [CVS PHARMACY] 6 Current NDC, Legacy NDC, 2 package rows 20250121_814ec7bf-f825-1095-e053-2a91aa0aee59.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 Marketing start Marketing end Sample Exclude flag Status 69842-353-29 69842035329 1 BOTTLE, WITH APPLICATOR in 1 CARTON (69842-353-29) / 14.7 mL in 1 BOTTLE, WITH APPLICATOR 2019-02-07 0000-00-00 No No Current