Home NDC 10157-2106 KANKA
Product NDC 10157-2106
11-digit product format 101572106
Labeler code 10157
Product ID 10157-2106_bbba35d9-5dd7-4471-ad62-63061a9128a1
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine and ZINC CHLORIDE
Dosage form GEL
Route ORAL
Labeler Blistex Inc
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-09-25
Substance BENZOCAINE; ZINC CHLORIDE
Active strength 20; .1 mg/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 KANKA
Brand name suffix SoftBrush
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 mg/100g ZINC CHLORIDE .1 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 86Q357L16B Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1249105 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 10157-2106-1 KANKA SoftBrush 2 g in 1 APPLICATOR GEL 2 2 10157-2106-1 KANKA SoftBrush 1 in 1 BLISTER PACK GEL 1 2 10157-2106-2 KANKA SoftBrush 2 g in 1 APPLICATOR GEL 2 2 10157-2106-2 KANKA SoftBrush 2 in 1 BLISTER PACK GEL 2 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10157-2106 KANKA SOFTBRUSH (BENZOCAINE AND ZINC CHLORIDE) GEL [BLISTEX INC] 2 Current NDC, Legacy NDC, 4 package rows 20241215_093f3545-1d8e-48a3-a533-e9c3ae6d740b.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 10157-2106-1 10157210601 1 APPLICATOR in 1 BLISTER PACK (10157-2106-1) / 2 g in 1 APPLICATOR 1 applicator 2019-09-25 0000-00-00 No No Current 10157-2106-2 10157210602 2 APPLICATOR in 1 BLISTER PACK (10157-2106-2) / 2 g in 1 APPLICATOR 2 applicator 2019-09-25 0000-00-00 No No Current