Home NDC 10157-2127 Kanka Triple Action
Product NDC 10157-2127
11-digit product format 101572127
Labeler code 10157
Product ID 10157-2127_225703ba-c471-4c9a-9c01-4b7f075b7878
Type HUMAN OTC DRUG
Nonproprietary name BENZOCAINE and MENTHOL, UNSPECIFIED FORM
Dosage form GEL
Route ORAL
Labeler Blistex Inc.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-06
Substance BENZOCAINE; MENTHOL, UNSPECIFIED FORM
Active strength 20; 2 g/100g; g/100g
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 Kanka Triple Action
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 g/100g MENTHOL, UNSPECIFIED FORM 2 g/100g
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 1006079 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 10157-2127-1 Kanka Triple Action 1 in 1 CARTON GEL 1 1 10157-2127-1 Kanka Triple Action 11.9 g in 1 TUBE GEL 11.9 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10157-2127 KANKA TRIPLE ACTION (BENZOCAINE AND MENTHOL, UNSPECIFIED FORM) GEL [BLISTEX INC.] 1 Current NDC, 2 package rows 20250112_078fcdab-38a1-4a9a-bdd3-e17446591ea8.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 Sample Exclude flag Status 10157-2127-1 10157212701 1 TUBE in 1 CARTON (10157-2127-1) / 11.9 g in 1 TUBE 1 tube 2025-01-06 No No Current