Official product label reference

Olu Pain Management — HAWAII REPACK, INC.

This page contains 12 source sections for LIDOCAINE AND CAMPHOR, cutaneous route. Label set 31ed3d82-ba12-46b2-b0ec-7e5e019efc10, version 2.

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

USES For the temporary relief of muscle pain and joint pain associated with: -Backache -Cramps -Soreness -Strains -Discomfort -Neckache

Purpose

PURPOSE Local Anesthetic PURPOSE Counterirritant

Dosage and administration — label text

DIRECTIONS Adults and Children 12 Years of Age and Older: -Clean and dry the affected area -Apply gel pad directly onto skin for up to 12 hours -Wash hands immediately after use -Gel pad can be cut into pieces and used on up to 2 body parts at a time -One application per day is recommended

Warnings

WARNINGS: FOR EXTERNAL USE ONLY

Active ingredient

ACTIVE INGREDIENTS Lidocaine 4% ACTIVE INGREDIENTS Camphor 1%

Unclassified section

ALLERGY ALERT Local anesthetics may cause methemoglobinemia. If an allergic reaction occurs, stop use and seek medical attention immediately. FLAMMABLE Keep away from excessive heat or open flame OTHER INFORMATION -Store in a cool, dry place with pouch tightly closed. Keep from freezing. -If the tamper-evident foil seal is not intact, do not use QUESTIONS OR COMMENTS info@olakinotherapeutics.com Distributed by: Hawaii Repack, Inc. 677 Ala Moana Blvd Ste 700, Honolulu, Hawaii-96813

Do not use

DO NOT USE -On damaged, irritated, or infected skin -With a bandage or heating pad -If you are allergic to any ingredients in this product -In the eyes, nose, or mouth -Otherwise as directed

While using this medicine

WHEN USING THIS PRODUCT Avoid contact with the eyes, nose, and mouth

When to stop use and seek help

STOP USE AND ASK DOCTOR IF -Any of the warnings apply to you -Excessive skin irritation develops -Condition worsens -Symptoms persist for more than 7 days, or symptoms clear up and occur again within 3 days

Pregnancy or breast feeding

IF PREGNANT OR BREASTFEEDING Ask a healthcare professional before use

Child safety

KEEP OUT OF REACH OF CHILDREN If ingested, seek medical help or contact Poison Control immediately

Inactive ingredient

INACTIVE INGREDIENTS Arnica Extract, Boswellia Extract, Vitamin C, Vitamin E, Ethyl Alcohol, Propylene Glycol, Glycerol, Sodium Polyacrylate, Tartaric Acid, Dihydroxyaluminium Aminoacetate, Methylparaben, Water

Official sources and product identifiers

DailyMed — complete source labelVerify the current version and original formatting, including tables and diagrams.
openFDA — structured source recordMachine-readable label source, linked by the exact label set ID.

Substances listed: CAMPHOR (NATURAL), LIDOCAINE

RxNorm identifiers: 2700664

Package NDC codes

85534-0102-0, 85534-0102-1

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.

Olu Pain Management drug information