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OTC products · Product label record

Lidocaine Pain Relief drug information

LIDOCAINE
Cardinal Health, 110 dba LEADER · TOPICAL

Product NDC: 70000-0741

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameLIDOCAINE
Labeler / manufacturerCardinal Health, 110 dba LEADER
RouteTOPICAL
Drug classAmide Local Anesthetic / Antiarrhythmic
Product NDC70000-0741
Label effective date2026-08-26

Official product label reference

Lidocaine Pain Relief — Cardinal Health, 110 dba LEADER

This page contains 13 source sections for LIDOCAINE, topical route. Label set 025d508b-ec4f-466c-b3e8-ba9b18d07b46, version 4.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Indications and Usage Uses: Temporaily relieves minor pains.

Purpose

Purpose External analgesic
Dosage and administration — label text
Dosage and Administration Directions ■ Adults and children 2 years of age and over: Clean and dry affected area, free of lotions, ointments and creams. Carefully remove backing from patch starting at a corner. Apply sticky side of patch to affected area. Do not use more than one patch in a i 2 hour period. Maximum 2 patches per day. Discard patch after single use. ■ Children under 2 years of age: Do not use, ask a doctor
Warnings
Warnings For external use only.
Active ingredient
Active Ingredients Lidocaine 4% . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Topical Anesthetic
While using this medicine
When using this product When using this product■avoid contact with the eyes ■ do not use more than one patch on your body ata time
When to stop use and seek help
Stop use and consult a doctor Stop use and ask a doctor if ■ skin irritation develops ■ condition worsens ■symptoms persist for more than 7 days or clear up and occur again within a few days
Pregnancy or breast feeding
If pregnant or breastfeeding, ask a health professional before use.
Do not use
Do not Use Over raw surfaces or blistered areas
Child safety
Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Other safety information
Other Safety Information Other information Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture. Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.
Inactive ingredient
Inactive Ingredients dihydroxy aluminium aminoacetate, disodium EDTA, glycerin, methylparaben, polyacrylic acid, polyvinyl alcohol, propyl paraben, propylene glycol, sodium carboxymethylcellulose, sodium polyacrylate, tartaric acid, titanium dioxide, water
Questions
Questions CALL TOLL-FREE 1-866-326-1313

Official sources and product identifiers

Substances listed: LIDOCAINE

RxNorm identifiers: 1737778

Package NDC codes

70000-0741-1, 70000-0741-2

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.