Label at a glance#

ProductExigence One Patch

Active ingredientLIDOCAINE, MENTHOL, UNSPECIFIED FORM

Label structure14 sections

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times a daily. Children under 2 years of age: consult a doctor.

Contacts and useful links#

PhoneLabel contact(310) 320-0100

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1%

OTC - PURPOSE SECTION

Topical Analgesic

USE

INDICATIONS & USAGE SECTION

For the temporary relief of pain.

WARNINGS SECTION

For external use only not intended for ingestion.

OTC - DO NOT USE SECTION

Do not use in large quantities, particularly over raw surfaces, or blistered areas.

OTC - WHEN USING SECTION

Avoid contact with the eyes.

STOP USE AND ASK DOCTOR

OTC - ASK DOCTOR SECTION

Stop use and ask doctor if condition worsens, or if symtoms persist for more than 7 days or clear up and occur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help, or contact a Poison Control Central right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times a daily.
Children under 2 years of age: consult a doctor.

OTHER SAFETY INFORMATION

Store at 20-25 ^oC (68-77 ^oF) and protect from moisture.

INACTIVE INGREDIENT SECTION

polyacrylamide, vinol, sodium polyacrylate; acrylate polymerization, purified water.

OTC - QUESTIONS SECTION

Questions?

(310) 320-0100

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

box

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1249758	Lidocaine/Menthol (Topical)	lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch	SCD Active

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
81902-102-01	EA - Each	81902-102	c086303e-c664-465a-9977-af52d8a35d7b	1	2021-09-07

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Exigence One Patch
Lidocaine 4%, Menthol 1%
POLYACRYLAMIDE (10000 MW)
ETHENYL
ACRYLATES CROSSPOLYMER-6
SODIUM POLYACRYLATE (2500000 MW)
LIDOCAINE
WATER
MENTHOL, UNSPECIFIED FORM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81902-102	81902-102-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POLYACRYLAMIDE (10000 MW)	E2KR9C9V2I	IACT
ETHENYL	PQ2K3G3591	IACT
ACRYLATES CROSSPOLYMER-6	4GXD0Q3OS3	IACT
SODIUM POLYACRYLATE (2500000 MW)	05I15JNI2J	IACT
LIDOCAINE	98PI200987	ACTIB
WATER	059QF0KO0R	IACT
MENTHOL, UNSPECIFIED FORM	L7T10EIP3A	ACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
06f11d1a-8131-97d6-e063-6294a90af031			c8b1a354-4ccf-42e5-e053-2a95a90ae1ab	2023-10-05	Warnings	Exact identifier spl set id: c8b1a354-4ccf-42e5-e053-2a95a90ae1ab

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Exigence One Patch