Home NDC 69842-623 PM Toothache Relief
Product NDC 69842-623
11-digit product format 698420623
Labeler code 69842
Product ID 69842-623_439566da-cc7b-d5bc-e063-6394a90a6b64
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form CREAM
Route DENTAL
Labeler CVS
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-11-17
Substance BENZOCAINE; MENTHOL; ZINC CHLORIDE; BENZALKONIUM CHLORIDE
Active strength 20; .26; .15; .13 g/100g; g/100g; g/100g; g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [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 PM Toothache Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 g/100g MENTHOL .26 g/100g ZINC CHLORIDE .15 g/100g BENZALKONIUM CHLORIDE .13 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2370903 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 69842-623-09 PM Toothache Relief 1 in 1 BOX CREAM 1 4 69842-623-09 PM Toothache Relief 7.1 g in 1 TUBE CREAM 7.1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-623 PM TOOTHACHE RELIEF (BENZOCAINE) CREAM [CVS] 2 Current NDC, 2 package rows 20250119_0a5a8cd0-d680-8a0f-e063-6294a90aa65c.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 109 of 153 · 3,057 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69842-623-09 69842062309 1 TUBE in 1 BOX (69842-623-09) / 7.1 g in 1 TUBE 1 tube 2023-11-17 No No Current