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OTC products · Product label record

Knee Pain Relief Roll-On drug information

LIDOCAINE AND MENTHOL
Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. · TOPICAL

Product NDC: 83602-375

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Generic nameLIDOCAINE AND MENTHOL
Labeler / manufacturerGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.
RouteTOPICAL
Drug classAmide Local Anesthetic / Antiarrhythmic
Product NDC83602-375
Label effective date2026-08-24

Official product label reference

Knee Pain Relief Roll-On — Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.

This page contains 14 source sections for LIDOCAINE AND MENTHOL, topical route. Label set 59c8b33a-7d4f-2c6e-e063-6394a90a7929, version 1.

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

Use Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.

Purpose

Purpose (Lidocaine) Topical Anesthetic (Menthol) Topical Analgesic
Dosage and administration — label text
Directions Adults and Children above 12 years old : · apply a thin layer to affected area every 6 to 8 hours, not more than 3 to 4 times daily · massage until thoroughly absorbed into skin · wash hands thoroughly with soap and water after each use · children under 12 years of age: ask a doctor
Warnings
Warnings For external use only
Active ingredient
Active Ingredient Lidocaine 4% ...... Purpose: Topical Anesthetic Menthol 1% ...... Purpose: Topical Analgesic
Do not use
Do not use · on wounds or on irritated or damaged skin · with a heating pad or device · with other ointments, creams, sprays, or liniments · if your are allergic to any ingredients of this product
While using this medicine
When using this product · use only as directed · avoid contact with the eyes, mucous membranes, or rashes · do not bandage tightly · do not expose the area to local heat or to direct sunlight
When to stop use and seek help
Stop use if · skin reactions such as redness, swelling, blistering or other discomfort occur · condition worsens or symptoms persist for more than 7 days · symptoms clear up and occur again within a few days · redness is present or excessive skin irritation occurs
Ask a doctor before use
Ask a doctor if · skin reactions such as redness, swelling, blistering or other discomfort occur · condition worsens or symptoms persist for more than 7 days · symptoms clear up and occur again within a few days · redness is present or excessive skin irritation occurs
Pregnancy or breast feeding
If pregnant or breast-feeding Ask a health professional before use
Child safety
Keep out of reach of children If swallowed accidentally , get medical help or contact with Poison Control Center immediately.
Other safety information
Other Information ·Store at 20°C to 25°C (68°F - 77°F) ·Store in a cool dry place away from direct sunlight
Inactive ingredient
Inactive Ingredients .ALPHA.-TOCOPHEROL, D-, Aloe Vera Extract, Carbomer, Isopropyl myristate, Lavender Oil, Phenoxyethanol, Polysorbate 80, Propylene Glycol, Tartaric acid, Water
Questions
Questions or Comments supports@sumifunofficial.com

Official sources and product identifiers

Substances listed: LIDOCAINE, MENTHOL

RxNorm identifiers: 1804176

Package NDC codes

83602-375-73

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.