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Pain relief - Medication Information

Product NDC Code 47682-321
Drug Name

Pain relief

Type Brand
Active Ingredients
Menthol 70 mg/l
Route TOPICAL
Dosage Form SPRAY
Application Number M015
Labeler Name Unifirst First Aid Corporation
Packages
Package NDC Code Description
47682-321-02 .059 l in 1 bottle, spray (47682-321-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients USP Menthol 7%

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 (2 years and older): Shake well and aply to affected araea not more than 3-4 times daily. Do not bandage tightly. Children under 2 years: Consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients coconut oil, eucalyptus lkeaf oil, glycerol, isopropyl alcohol, peppermint oil, water, wintergreen leaf oil

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 of minor aches and pains of muscles and joints.

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.
Pain Relief Analgesic Menthol COCONUT OIL MENTHOL MENTHOL ISOPROPYL ALCOHOL EUCALYPTUS OIL GLYCERIN WATER METHYL SALICYLATE PEPPERMINT OIL PEPPERMINT

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.
Green Guard Pain Relief Spray Label Pain Relief spray Fast Acting pain Relief For Temporary Relief of Minor Aches and Pains Green Guard® 2 Fl. Oz. (59.1 mL) Green Guard

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

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 are prone to allergic reactions to salicylates, including aspirin

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 open wounds or damaged 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 swallowed, get medical help or contact a Poison Control Center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information store at room temperature 56°-86°F (15°-30°C) will not stain clothing

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? 1-800-869-6970

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 symptoms persist for more than 7 days or clear up and recur again within a few days excessive skin irritation occurs

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 avoid contact with eyes

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast feeding, ask a doctor 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. Flammable. Keep away from flame. Do not use on open wounds or damaged skin Ask a doctor before use if you are prone to allergic reactions to salicylates, including aspirin When using this product avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and recur again within a few days excessive skin irritation occurs

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