Home NDC 0363-1623 PM Toothache Relief
Product NDC 0363-1623
11-digit product format 003631623
Labeler code 0363
Product ID 0363-1623_43956f49-90bc-5b18-e063-6294a90aad71
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form PASTE
Route DENTAL
Labeler Walgreens
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-10-27
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 0363-1623-09 PM Toothache Relief 7.1 g in 1 TUBE PASTE 7.1 6 0363-1623-09 PM Toothache Relief 1 in 1 BOX PASTE 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-1623 PM TOOTHACHE RELIEF (BENZOCAINE) PASTE [WALGREENS] 4 Current NDC, Legacy NDC, 2 package rows 20250119_e816f742-fba9-3c12-e053-2a95a90a192f.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 18 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 Marketing end Sample Exclude flag Status 0363-1623-09 00363162309 1 TUBE in 1 BOX (0363-1623-09) / 7.1 g in 1 TUBE 1 tube 2022-10-28 0000-00-00 No No Current