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Menthol pain relief gel-roll on - Medication Information

Product NDC Code 83602-333
Drug Name

Menthol pain relief gel-roll on

Type Brand
Active Ingredients
Menthol .04 g/ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 415974
Application Number M017
Labeler Name Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
Packages
Package NDC Code Description
83602-333-25 74 ml in 1 bottle (83602-333-25)
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Menthol 4% ...... Purpose: Topical Analgesic

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 Adults and children 12 years of age and older: • Rub a thin film over affected areas not more than 4 times daily; • Message not necessary Children under 12 years of age: Consult physician. Wash hands after use with cool water.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Alcohol, Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Boswellia Carterii Resin Extract, Camellia Sinensis Leaf Extract, Carbomer, Camphor, FD&C Blue 1, FD&C Yellow 5, Glycerin, Isopropyl Myristate, Ilex Paraguariensis Leaf Extract, Silica, Triethanolamine, Vitamin E, 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 Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, ankle, back, neck, hips, shoulders, elbows.

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-Roll On Menthol ALCOHOL 95% MENTHOL MENTHOL TROLAMINE WATER SILICON DIOXIDE ILEX PARAGUARIENSIS LEAF ISOPROPYL MYRISTATE .ALPHA.-TOCOPHEROL, D- ALOE VERA LEAF GLYCERIN FD&C YELLOW NO. 5 FD&C BLUE NO. 1 GREEN TEA LEAF CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE FRANKINCENSE ARNICA MONTANA FLOWER CAMPHOR (SYNTHETIC)

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.
Container Label Package Label

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 if • skin reactions such as redness, swelling, blistering or other discomfort occur • symptoms persist for more than 7 days

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use • on wounds or damaged skin • with a heating pad or device • with other ointments, creams, sprays, or liniments • if you are allergic to any ingredients of this product

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 swallowed accidentally, get medical help or contact with 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: [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 ... if • skin reactions such as redness, swelling, blistering or other discomfort occur • symptoms persist for more than 7 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 • avoid contact with the eyes, mucous membranes, or rashes • do not bandage tightly

Pregnancy or breast feeding

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

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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