Blistex

Product NDC: 10157-9302
11-digit product format: 101579302
Labeler code: 10157
Product ID: 10157-9302_78fbbd4f-548d-4b5a-8e15-2ae2a01a3592
Type: HUMAN OTC DRUG
Nonproprietary name: Benzocaine and Chloroxylenol
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Blistex Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-03-05
Substance: BENZOCAINE; CHLOROXYLENOL
Active strength: 5; .1 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: Blistex
Brand name suffix: Foille Medicated First Aid
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZOCAINE	5 g/100g
CHLOROXYLENOL	.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
0F32U78V2Q	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
199005	Internal RxNorm lookup
213034	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
e2eca808-e97b-43e0-aa51-7025cc61c7a8	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
10157-9302-3	Blistex Foille Medicated First Aid	1 in 1 CARTON	OINTMENT	1	4
10157-9302-3	Blistex Foille Medicated First Aid	14 g in 1 TUBE	OINTMENT	14	4
10157-9302-4	Blistex Foille Medicated First Aid	1 in 1 CARTON	OINTMENT	1	4
10157-9302-4	Blistex Foille Medicated First Aid	28 g in 1 TUBE	OINTMENT	28	4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Benzocaine	ACTIVE INGREDIENT	U3RSY48JW5	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
Chloroxylenol	ACTIVE INGREDIENT	0F32U78V2Q	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
Benzocaine	ACTIVE MOIETY	U3RSY48JW5	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
Chloroxylenol	ACTIVE MOIETY	0F32U78V2Q	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
calcium hydroxide	INACTIVE INGREDIENT	PF5DZW74VN	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
ceresin	INACTIVE INGREDIENT	Q1LS2UJO3A	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
corn oil	INACTIVE INGREDIENT	8470G57WFM	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
edetate calcium disodium anhydrous	INACTIVE INGREDIENT	8U5D034955	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
eugenol	INACTIVE INGREDIENT	3T8H1794QW	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
maleic anhydride	INACTIVE INGREDIENT	V5877ZJZ25	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
polyethylene glycol 1500	INACTIVE INGREDIENT	1212Z7S33A	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
sodium borate	INACTIVE INGREDIENT	91MBZ8H3QO	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
water	INACTIVE INGREDIENT	059QF0KO0R	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1
yellow wax	INACTIVE INGREDIENT	2ZA36H0S2V	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10157-9302	BLISTEX FOILLE MEDICATED FIRST AID (BENZOCAINE AND CHLOROXYLENOL) OINTMENT [BLISTEX INC.]	4	Current NDC, Legacy NDC, 4 package rows	20241213_e2eca808-e97b-43e0-aa51-7025cc61c7a8.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 55 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Magsoothium Body	MENTHOL, CAPSAICIN	Ubu/Elements, Inc.	f604d30c-b17c-ec01-e053-2a95a90aa304	2025-12-15	Warnings	Exact identifier application number: M017
Salonpas pain relieving JET	MENTHOL, METHYL SALICYLATE	Hisamitsu Pharmaceutical Co., Inc.	dd1ea3bf-891a-402e-8f43-14302bc9c3e5	2025-12-15	Warnings	Exact identifier application number: M017
Herbal Tendon Bone Relief	CAMPHOR MINT	Guchutang Biotechnology (Longyan) Co., Ltd.	45cf4040-9751-d24b-e063-6294a90aff27	2025-12-13	Warnings	Exact identifier application number: M017
ElixirLidoFast	LIDOCAINE 5% CREAM	ELIXIR HEALTHCARE USA, LLC.	45de5a3d-06c2-aa02-e063-6294a90a63d3	2025-12-13	Warnings	Exact identifier application number: M017
MEDI FIRST PLUS	HYDROCORTISONE ACETATE	Orazen Inc	5781124a-60f4-4a64-80b7-ce5f28d495b5	2025-12-12	Warnings	Exact identifier application number: M017
MEDI-FIRST	HYDROCORTISONE ACETATE	Orazen Inc	aeffd85c-58a7-4d64-bf94-977b6fbbe713	2025-12-12	Warnings	Exact identifier application number: M017
Joint and Muscle Relief	MENTHOL	Smart Cookie Solutions Inc.	45c24d56-4dc9-2884-e063-6294a90a52cc	2025-12-12	Warnings	Exact identifier application number: M017
Popstar	DELAY SPRAY	Pineapple Brands LLC	293b2da9-1261-0358-e063-6394a90aa08c	2025-12-12	Warnings	Exact identifier application number: M017
Careland Pain Relief Plus	CAMPHOR, MENTHOL, METHYL SALICYLATE	Planet (Anhui) Pharmaceutical Co., Ltd.	d9e63ddd-d003-45fa-b156-7f4452c28cbd	2025-12-12	Warnings	Exact identifier application number: M017
Glucosamine Cream EXTRA STRENGTH	HISTAMINE DIHYDROCHLORIDE	IDEAZ, LLC	f4d414b7-89e7-ad65-e053-2a95a90a25d4	2025-12-12	Warnings	Exact identifier application number: M017
ARTHRITIS	MENTHOL	Smith Amish, LLC	20c36972-b695-1241-e063-6394a90adf63	2025-12-12	Warnings	Exact identifier application number: M017
FOOT	MENTHOL	Smith Amish, LLC	20c48537-f55f-c10f-e063-6394a90a4cca	2025-12-12	Warnings	Exact identifier application number: M017
Joint Ease	MENTHOL	Smith Amish, LLC	20c4a0f8-bdc6-d89a-e063-6294a90aa8d8	2025-12-12	Warnings	Exact identifier application number: M017
Toast Screamin Hot	CAPSAICIN	IDEAZ, LLC	331207e6-b8ac-b169-e063-6394a90ac169	2025-12-12	Warnings	Exact identifier application number: M017
Pain Relief Gel-Patch	LIDOCAINE	KORVIA GLOBAL Inc.	45ccfcae-a307-1c5f-e063-6294a90acf89	2025-12-12	Warnings	Exact identifier application number: M017
Lidospot patch	LIDOCAINE AND MENTHOL	Fabrication Enterprises Inc	3a6e94c4-1ca6-e77a-e063-6394a90a4bfc	2025-12-12	Warnings	Exact identifier application number: M017
LETEBEE LIGHT neuropathy pain relief cream for feet	MENTHOL	Guangdong Aimu Biological Technology Co., Ltd	45a99afc-15ec-76c2-e063-6294a90a2220	2025-12-11	Warnings	Exact identifier application number: M017
Cinthera	LIDOCAINE	Strand Health Group	2746e5b2-be2d-f2d2-e063-6394a90a3690	2025-12-11	Warnings	Exact identifier application number: M017
Equate Cool and Heat Pain Relieving Liquid	COOL AND HEAT PAIN RELIEF	Walmart, Inc.	ad156685-3bd5-6837-e053-2995a90ac788	2025-12-11	Warnings	Exact identifier application number: M017
HUMCO Camphor Spirit	CAMPHOR 10%	Humco Holding Group, Inc.	9a0ef0a3-3c79-41b2-8193-424a3ef9886f	2025-12-11	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
U3RSY48JW5	BENZOCAINE	94-09-7	BENZOCAINE
0F32U78V2Q	CHLOROXYLENOL	88-04-0	CHLOROXYLENOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
199005	benzocaine 5 % / chloroxylenol 0.1 % Topical Ointment	PSN	e2eca808-e97b-43e0-aa51-7025cc61c7a8	4
213034	Foille 5 % / 0.1 % Topical Ointment	PSN	e2eca808-e97b-43e0-aa51-7025cc61c7a8	4
213034	benzocaine 0.05 MG/MG / chloroxylenol 0.001 MG/MG Topical Ointment [Foille]	SBD	e2eca808-e97b-43e0-aa51-7025cc61c7a8	4
199005	benzocaine 0.05 MG/MG / chloroxylenol 0.001 MG/MG Topical Ointment	SCD	e2eca808-e97b-43e0-aa51-7025cc61c7a8	4
199005	benzocaine 5 % / chloroxylenol 0.1 % Topical Ointment	SY	e2eca808-e97b-43e0-aa51-7025cc61c7a8	4
213034	Foille (benzocaine 5 % / chloroxylenol 0.1 % ) Topical Ointment	SY	e2eca808-e97b-43e0-aa51-7025cc61c7a8	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
10157-9302-3	10157930203	1 TUBE in 1 CARTON (10157-9302-3) / 14 g in 1 TUBE	1 tube	2016-09-23	0000-00-00	No	No	Current
10157-9302-4	10157930204	1 TUBE in 1 CARTON (10157-9302-4) / 28 g in 1 TUBE	1 tube	2013-03-05	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Blistex ® Foille ® Medicated First Aid Ointment	Blistex Inc.	2024-12-11	HUMAN OTC DRUG LABEL	4
4357 First Aid Kit	Honeywell Safety Products USA, INC	2024-01-22	HUMAN OTC DRUG LABEL	7
4379 First Aid Kit	Honeywell Safety Products USA, INC	2024-01-22	HUMAN OTC DRUG LABEL	7
4246 First Aid Kit	Honeywell Safety Products USA, INC	2021-12-23	HUMAN OTC DRUG LABEL	4
4358 First Aid Kit	Honeywell Safety Products USA, INC	2021-12-23	HUMAN OTC DRUG LABEL	4