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Biofreeze pain relief - Medication Information

Product NDC Code 59316-307
Drug Name

Biofreeze pain relief

Type Brand
Active Ingredients
Menthol, unspecified form 100 mg/ml
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 253020,
2001133
Application Number part348
Labeler Name RB Health (US) LLC
Packages
Package NDC Code Description
59316-307-10 1 jar in 1 carton (59316-307-10) / 89 ml in 1 jar
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingreidents Menthol 10% Purpose Cooling Pain Relief

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; massage not necessary. Childern under 12 years of age: Consult physician

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Caprylic/Capric Triglyceride, Cetearyl Alcohol, Diazolidinyl Urea, Dimethicone, Gluconolactone, Glycerin, Glyceryl Stearate, Ilex Paraguariensis Leaf Extract, Iodopropynyl butylcarbamate, Polysorbate 60, Sodium Benzoate, Sodium Hydroxide, Sodium Stearoyl Lactylate, Tetrasodium EDTA, Tocopheryl Acetate, Vitis Vinifera (Grape) seed Oil, 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 arthritis, backache, strains, and sprains

Purpose

Information about the drug product’s indications for use.
Purpose Cooling Pain Relief

Spl product data elements

Usually a list of ingredients in a drug product.
Biofreeze Pain Relief MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM TRICAPRIN CETOSTEARYL ALCOHOL DIAZOLIDINYL UREA DIMETHICONE GLUCONOLACTONE GLYCERIN GLYCERYL MONOSTEARATE ILEX PARAGUARIENSIS LEAF IODOPROPYNYL BUTYLCARBAMATE POLYSORBATE 60 SODIUM BENZOATE SODIUM HYDROXIDE SODIUM STEAROYL LACTYLATE EDETATE SODIUM .ALPHA.-TOCOPHEROL ACETATE GRAPE SEED OIL WATER

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: Label10 Label11

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 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 Contropl 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 1-800-246-3733

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 recur

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 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 or if excessive irritation develops Do not bandage Wash hands after use with cool water Do not use with heating pad or device Store in a cool dry place

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breat-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. Ask a doctor before use if you have: Sensitive skin When using this product: 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 or if excessive irritation develops Do not bandage Wash hands after use with cool water Do not use with heating pad or device Store in a cool dry place Stop use and ask a doctor if: Condition worsens, or if symptoms persist for more than 7 days, or clear up and recur If pregnant or breat-feeding: Ask a health professional before use Keep out of reach of children: If accidentally ingested, get medical help or contact a Poison Contropl Center immediately

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