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Stopain clinical - Medication Information

Product NDC Code 63936-9758
Drug Name

Stopain clinical

Type Brand
Active Ingredients
Menthol 100 mg/g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 259249,
1865942
Application Number M017
Labeler Name Troy Manufacturing, Inc.
Packages
Package NDC Code Description
63936-9758-1 3 g in 1 packet (63936-9758-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Menthol 10.0% 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 over 12 years: ask a doctor.​​ ​Children 12 years or younger: apply directly onto affected area without the need to bandage repeat if necessary, but do not apply more than 4 times daily.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients acrylic acid/vinyl ester copolymer, dimethylsulfone (MSM), eucalyptus oil, glucosamine sulfate, hydroxypropylcellulose, PEG-8 dimethicone, pentylene glycol, peppermint oil, SD alcohol 39C, triethanolamine, water (USP).

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 For the temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises 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.
Stopain Clinical MENTHOL ACRYLIC ACID DIMETHYL SULFONE EUCALYPTUS OIL GLUCOSAMINE SULFATE HYDROXYPROPYL CELLULOSE, UNSPECIFIED PEG-8 DIMETHICONE PENTYLENE GLYCOL PEPPERMINT OIL TROLAMINE WATER 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.
Package Labeling: Packet

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts Other Information Store at room temperature

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, get medical help or contact a Poison Control Center right away.

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 condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days redness is present excessive irritation of the skin develops

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 a heating pad do not apply to wounds or damaged skin

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 ​Avoid contact with eyes. ​For external use only. Flammable: Keep away from fire or flame. When using this product use only as directed do not bandage tightly or use a heating pad do not apply to wounds or damaged skin Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days redness is present excessive irritation of the skin develops If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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