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Cvs pain relief - Medication Information

Product NDC Code 51316-161
Drug Name

Cvs pain relief

Type Brand
Active Ingredients
Menthol, (+)- 4 g/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 415974
Application Number M017
Labeler Name CVS
Packages
Package NDC Code Description
51316-161-02 74 ml in 1 bottle, plastic (51316-161-02)
51316-161-03 89 ml in 1 tube (51316-161-03)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Menthol 4%

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.
Adults and children of 12 years: rub a thin film over affected area not more than 3 to 4 times daily. Children under 12 years of age: ask a doctor. Wash hands after use with cool water.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Carbomer, fragrance, isopropyl alcohol, magnesium sulfate, sodium hydroxide, 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.
Temporarily relieves minor aches and pains of muscles and joints associated with arthritis, simple backache, sprains, bruises, and muscle strains.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
CVS Pain Relief Menthol 4% CARBOMER 940 WATER MENTHOL, (+)- MENTHOL, (+)- SODIUM HYDROXIDE ISOPROPYL ALCOHOL MAGNESIUM SULFATE, UNSPECIFIED

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.
Label Label

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.
If product is swallowed, get medical help or contact a Poison Control Center right away.

Pregnancy or breast feeding

Pregnancy 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.
For external use only. Flammable. Keep away from excessive heat or open flame. When using this product use only as directed. Avoid contact with eyes and mucous membranes, do not apply to wounds or damaged skin, do no apply to irritated skin or if excessive irritation develops, do not bandage tightly or use with heating pad or device. Children 12 years of age and older: use only under adult supervision. Stop use and ask a doctor if you experience pain, swelling, or blistering of the skin, condition worsens, symptoms last more than 7 days or clear up and occur again within a few days.

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