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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
eebc03ba-f849-4e70-a653-834f383b6aa4	Available on FDA.report

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#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Benzocaine	ACTIVE INGREDIENT	U3RSY48JW5	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
Benzocaine	ACTIVE MOIETY	U3RSY48JW5	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
CASTOR OIL	INACTIVE INGREDIENT	D5340Y2I9G	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
CETYLPYRIDINIUM CHLORIDE	INACTIVE INGREDIENT	D9OM4SK49P	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
DIMETHYL ISOSORBIDE	INACTIVE INGREDIENT	SA6A6V432S	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
ETHYLCELLULOSES	INACTIVE INGREDIENT	7Z8S9VYZ4B	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
OLETH-10	INACTIVE INGREDIENT	JD797EF70J	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
POLYETHYLENE GLYCOL 300	INACTIVE INGREDIENT	5655G9Y8AQ	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
SUCRALOSE	INACTIVE INGREDIENT	96K6UQ3ZD4	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1
TANNIC ACID	INACTIVE INGREDIENT	28F9E0DJY6	KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.]	1

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 16 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GuruNanda Oxyfusion	HYDROGEN PEROXIDE	GURUNANDA, LLC	3be317b9-a5d8-b198-e063-6394a90af985	2025-11-11	Warnings	Exact identifier application number: M022
GuruNanda Oral Pain Relief	MENTHOL	GURUNANDA, LLC	3b8f3562-0e46-bea4-e063-6294a90adb71	2025-11-11	Warnings	Exact identifier application number: M022
TopCare Cherry Flavor	PHENOL	TOPCO ASSOCIATES, LLC	5d3f0610-deb4-4180-ae19-2c65ed2f368b	2025-11-10	Warnings	Exact identifier application number: M022
Topcare Sore Throat Menthol Flavor	PHENOL	TOPCO ASSOCIATES LLC	fb1f2c11-2508-4985-bae5-7d547bd6aa23	2025-11-10	Warnings	Exact identifier application number: M022
Zilactin-B	BENZOCAINE	ASCENT CONSUMER PRODUCTS, INC	42eeb3d4-bac6-4e29-e063-6294a90a644d	2025-11-06	Warnings	Exact identifier application number: M022
Zilactin Early Relief Cold Sore	BENZYL ALCOHOL	ASCENT CONSUMER PRODUCTS, INC	42ef8bfa-c4d9-01cf-e063-6394a90ac88a	2025-11-06	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic Gel	BENZOCAINE	Beutlich Pharmaceuticals, LLC	106b6115-d043-4050-80c6-1d82456dea02	2025-11-06	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic Gel	BENZOCAINE	Beutlich Pharmaceuticals, LLC	4c278122-2643-46bf-9e44-11985210a16e	2025-11-06	Warnings	Exact identifier application number: M022
HurriCaine Topical Anesthetic Liquid	BENZOCAINE	Beutlich Pharmaceuticals, LLC	fee9969d-ad1a-4f44-9741-a0a44c9e1128	2025-11-06	Warnings	Exact identifier application number: M022
Ear Wax Removal Aid Drops	CARBAMIDE PEROXIDE	Target Corporation	0ddf9945-147d-4b25-98a6-4e9f12a4656f	2025-11-05	Warnings	Exact identifier application number: M022
Alpha-Caine Topical Anesthetic	BENZOCAINE	Dental Technologies, Inc.	e6a312e5-17ac-46f0-8723-4e40eeecd69f	2025-11-04	Warnings	Exact identifier application number: M022
PEROXY SHIELD MOUTH SORE	1.5% HYDROGEN PEROXIDE	Dental Technologies, Inc.	a72e433b-1b7d-4a0c-e053-2995a90a30c4	2025-11-04	Warnings	Exact identifier application number: M022
Alpha-Caine Topical Anesthetic	BENZOCAINE	Dental Technologies, Inc.	ae628766-25b7-4b4f-abb8-a43faf2f44b9	2025-11-04	Warnings	Exact identifier application number: M022
Alpha-Caine Topical Anesthetic	BENZOCAINE	Dental Technologies, Inc.	719743f9-21fc-4568-b879-acdfa4639464	2025-11-04	Warnings	Exact identifier application number: M022
Alpha-Caine Topical Anesthetic	BENZOCAINE	Dental Technologies, Inc.	ff0695a1-1d7d-4b51-97fd-689e56d914fe	2025-11-04	Warnings	Exact identifier application number: M022
Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Family Dollar (FAMILY WELLNESS)	f7edf75c-cdba-4dde-bfc5-a04af34759d3	2025-11-03	Warnings	Exact identifier application number: M022
7 Select Oral Pain Maximum Strength Relief	BENZOCAINE	7-ELEVEN, INC.	f170a570-1c50-4b9a-be16-9b01bf5eaa74	2025-10-31	Warnings	Exact identifier application number: M022
Oral Pain Relief	BENZOCAINE AND BENZALKONIUM CHLORIDE	Universal Distribution Center LLC	18520f9b-4d35-1e9c-e063-6294a90aaa39	2025-10-30	Warnings	Exact identifier application number: M022
Iodent Oral Analgesic	BENZOCAINE	United Exchange Corp.	63902125-f8dc-0ada-e053-2991aa0a7ce5	2025-10-30	Warnings	Exact identifier application number: M022
Ear Wax Removal Aid Drops	CARBAMIDE PEROXIDE	BETTER LIVING BRANDS, LLC	3bded237-4d2c-4b38-bedc-267fdc374194	2025-10-29	Warnings	Exact identifier application number: M022

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
U3RSY48JW5	BENZOCAINE	94-09-7	BENZOCAINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
308657	benzocaine 20 % Mucous Membrane Topical Solution	PSN	eebc03ba-f849-4e70-a653-834f383b6aa4	5
308657	benzocaine 200 MG/ML Mucous Membrane Topical Solution	SCD	eebc03ba-f849-4e70-a653-834f383b6aa4	5
308657	benzocaine 20 % Mucous Membrane Topical Solution	SY	eebc03ba-f849-4e70-a653-834f383b6aa4	5

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