Home NDC 55910-346 Rexall
Product NDC 55910-346
11-digit product format 559100346
Labeler code 55910
Product ID 55910-346_3c30c101-f57c-f3ba-e063-6394a90ac007
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form LIQUID
Route ORAL
Labeler Rexall
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-01-01
Substance BENZOCAINE
Active strength 20 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 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 Rexall
Brand name suffix Maximum Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 g/100mL
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55910-346-79 RexallMaximum Strength 14.7 mL in 1 BOTTLE LIQUID 14.7 11 55910-346-79 RexallMaximum Strength 1 in 1 CARTON LIQUID 1 11
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-346 REXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL] 10 Current NDC, Legacy NDC, 2 package rows 20250119_8f6e2780-cfb7-4bef-9b7d-13cb80d8923e.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 55910-346-69 55910034669 1 BOTTLE in 1 CARTON (55910-346-69) > 14.7 mL in 1 BOTTLE (55910-346-61) 1 bottle 2015-01-13 0000-00-00 No No Current 55910-346-79 55910034679 1 BOTTLE in 1 CARTON (55910-346-79) / 14.7 mL in 1 BOTTLE 1 bottle 2023-02-01 No No Current