Home NDC 10157-9477 Kank-A
Product NDC 10157-9477
11-digit product format 101579477
Labeler code 10157
Product ID 10157-9477_55568382-5b9f-4bc1-9532-38fb810532d3
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form LIQUID
Route BUCCAL
Labeler Blistex Inc.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-12-01
Substance BENZOCAINE
Active strength 200 mg/mL
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 Kank-A
Brand name suffix Mouth Pain
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/mL
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 10157-9477-1 Kank-A Mouth Pain 9.75 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 9.75 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10157-9477 KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.] 5 Current NDC, Legacy NDC, 1 package rows 20241220_eebc03ba-f849-4e70-a653-834f383b6aa4.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 32 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 10157-9477-1 10157947701 9.75 mL in 1 BOTTLE, WITH APPLICATOR (10157-9477-1) 9.75 ml 2011-12-01 0000-00-00 No No Current