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Menthol pain relief gel-patch - Medication Information

Product NDC Code 73557-131
Drug Name

Menthol pain relief gel-patch

Type Brand
Active Ingredients
Menthol .05 g/g
Route TOPICAL
Dosage Form PATCH
RxCUI drug identifier 420222
Application Number M017
Labeler Name Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
Packages
Package NDC Code Description
73557-131-05 5 patch in 1 box (73557-131-05) / 11 g in 1 patch (73557-131-02)
73557-131-16 15 patch in 1 box (73557-131-16) / 11 g in 1 patch (73557-131-02)
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Menthol 5.0%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions · Adult and Children 12 years of age and older: Clean and dry affected area, partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing patch to skin and leave in place for up to 8 hours. Use on affected areas not more than 4 times daily. Wash hands with cool water after use. · Children under 12 years of age : Consult physician

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Boswellia Carterii Resin Extract, Camellia Sinensis Leaf Extract, Carboxymethylcellulose Sodium, Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Hydroxyacetophenone, Kaolin, L-Tartaric Acid, Mineral Oil, Petrolatum, Polyacrylic Acid, Polysorbate 80, Propylene Glycol, PVP, Sodium Polyacrylate, Titanium dioxide, Water

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses: Temporary relief from minor aches and pains of sore muscles and joints associated with: · arthrits · backache · strains · sprains

Purpose

Information about the drug product’s indications for use.
Purpose Topical Analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
MENTHOL PAIN RELIEF Gel-Patch Menthol ARNICA MONTANA FLOWER FRANKINCENSE KAOLIN TARTARIC ACID WATER DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS PROPYLENE GLYCOL POLYACRYLIC ACID (250000 MW) CARBOXYMETHYLCELLULOSE SODIUM SODIUM POLYACRYLATE (2500000 MW) TITANIUM DIOXIDE MINERAL OIL PETROLATUM HYDROXYACETOPHENONE POLYSORBATE 80 GLYCERIN POVIDONE K90 GREEN TEA LEAF ALOE VERA LEAF EDETATE DISODIUM MENTHOL MENTHOL

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
02 05 16

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have: Sensitive skin

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children: If accidentally ingested, get medical help or contact a Poison Control Center immediately

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or Comments: 1 646-223-0128 · [email protected]

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if: Burning disconfort or excessive skin irritation develops, condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product: · Use only as directed · Do not bandage tightly or use with heating pad or device · Avoid contact with eyes or mucous membranes · Do not apply to wounds or damaged skin · Do not use with other ointments, creams, sprays, or liniments · Do not apply to irritated skin · Store in a cool dry place away from direct sunlight

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding: Ask a health professional before use

Storage and handling

Information about safe storage and handling of the drug product.
· Store in a cool dry place away from direct sunlight

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API

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