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 61 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nighttime 4X Medicated Cream	BENZOCAINE	Rite Aid	21645ed1-2dc0-223a-e063-6394a90ab021	2025-11-21	Warnings	Exact identifier application number: M017
4x Medicated Gum Cream	BENZOCAINE	Albertsons	b81a308c-9c30-0e3d-e053-2a95a90a15d2	2025-11-21	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET NOVELTIES, INC	b0edd9d9-951f-d3dd-e053-2995a90a8d5a	2025-11-21	Warnings	Exact identifier application number: M017
Up up	LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES	Target Corporation	44121d40-86e1-0df6-e063-6294a90aedaf	2025-11-20	Warnings	Exact identifier application number: M017
Up up	PAIN RELIEF ADVANCED HYDROGEL PATCHES	Target Corporation	44128b70-3172-ee37-e063-6294a90a705f	2025-11-20	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET NOVELTIES, INC	f03090fa-f7e6-f53a-e053-2a95a90aa819	2025-11-20	Warnings	Exact identifier application number: M017
HEATING PAIN RELIEF	METHYL SALICYLATE, MENTHOL	SUNSET NOVELTIES, INC	ff073e47-3107-e17e-e053-6294a90a58fa	2025-11-20	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET NOVELTIES, INC	fc8a8f20-97ab-481e-e053-6394a90a3525	2025-11-20	Warnings	Exact identifier application number: M017
MENTHOL	MENTHOL	SUNSET PAIN RELIEF ROLL-ON 3OZ	934d4638-b47b-187d-e053-2995a90ae69d	2025-11-20	Warnings	Exact identifier application number: M017
FOOT PAIN RELIEF ROLL-ON	LIDOCAINE, MENTHOL	Guangzhou Zhupuyou E-commerce Co., Ltd	43edcea0-ab04-f368-e063-6294a90a817a	2025-11-19	Warnings	Exact identifier application number: M017
Absolut Skin Corticosoothe Anti-Itch	HYDROCORTISONE	Absolut Skin Incorporated	deb52218-9176-4aaa-a22f-b66dada6690f	2025-11-19	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy	LIDOCAINE	InterMed Laboratories Private Limited	43f3d189-f6b7-02ed-e063-6394a90afd73	2025-11-19	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch HealthA2Z	LIDOCAINE	InterMed Laboratories Private Limited	43f3e288-e828-8130-e063-6394a90a6d44	2025-11-19	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch Leader	LIDOCAINE	InterMed Laboratories Private Limited	42f06914-c8b8-ea9c-e063-6294a90a79e6	2025-11-19	Warnings	Exact identifier application number: M017
CVS Anti-Itch	CAMPHOR, MENTHOL	CVS	87715662-c788-9a8d-e053-2a95a90acb53	2025-11-19	Warnings	Exact identifier application number: M017
Walgreen Anti Itch	CAMPHOR, MENTHOL	Walgreens	b4f47a8d-d4a6-9233-e053-2a95a90afd90	2025-11-19	Warnings	Exact identifier application number: M017
Leader Anti-Itch	CAMPHOR, MENTHOL	LEADER/Cardinal Helath 110, Inc.	9ca985c6-5017-0558-e053-2995a90a8202	2025-11-19	Warnings	Exact identifier application number: M017
CVS Anti-Itch	PRAMOXINE HCL	CVS	87fc476a-5b12-7383-e053-2995a90a530b	2025-11-19	Warnings	Exact identifier application number: M017
Walgreen Anti-Itch	PRAMOXINE HCL	Walgreens	b5f9d1c5-891e-4377-e053-2995a90aa281	2025-11-19	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET PAIN RELIEF	89f5f688-856f-f2df-e053-2995a90a73cf	2025-11-19	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