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| Product NDC Code | 59316-832 | ||||
|---|---|---|---|---|---|
| Drug Name | Biofreeze day and overnight |
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| Type | Brand | ||||
| Dosage Form | KIT | ||||
| RxCUI drug identifier | 420222, 2109627 |
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| Application Number | part348 | ||||
| Labeler Name | RB Health (US) LLC | ||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Menthol 5% Pain Relieving Patch
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: Clean and dry affected area, pop apart and partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing the patch to skin and leave in place for up to 8 hours. Use on affected area not more than 3 to 4 times daily. ■ children under 12 years of age : consult a physician ■wash hands after use with cool water
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Large Patch: 1,2-Hexanediol, Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Boswellia Carterii Resin Extract, Camellia Sinensis Leaf Extract, Carboxymethylcellulose Sodium, DihydroxyaluminumAminoacetate, Ethylhexylglycerin, Glycerin, Iodopropynyl Butylcarbamate, Kaolin, Mineral Oil, Petrolatum, Phenoxyethanol, Polyacrylic Acid, Polysorbate 80, Povidone, Propylene Glycol, PurifiedWater, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide Overnight Relief Patch: Benzalkonium Chloride, Carboxymethylcellulose Sodium, Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Kaolin, Lauralkonium Chloride, Lavender Oil, Mineral Oil, Petrolatum, Polyacrylic Acid, Polysorbate 80, Povidone, Propylene Glycol, Purified Water, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide
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 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.Menthol 5% Purpose: Pain Relieving Patch
Spl product data elements
Usually a list of ingredients in a drug product.Biofreeze Day and Overnight Menthol Biofreeze Overnight Relief Menthol, Unspecified Form LAURALKONIUM CHLORIDE TARTARIC ACID POLYACRYLIC ACID (450000 MW) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED EDETATE DISODIUM GLYCERIN MINERAL OIL POLYSORBATE 80 PROPYLENE GLYCOL POVIDONE, UNSPECIFIED TITANIUM DIOXIDE BENZALKONIUM CHLORIDE KAOLIN DIHYDROXYALUMINUM AMINOACETATE LAVENDER OIL PETROLATUM SODIUM POLYACRYLATE (2500000 MW) WATER MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM Biofreeze Menthol Menthol, Unspecified Form WATER 1,2-HEXANEDIOL PHENOXYETHANOL PETROLATUM GLYCERIN MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM ARNICA MONTANA FLOWER MINERAL OIL POVIDONE, UNSPECIFIED CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED ETHYLHEXYLGLYCERIN GREEN TEA LEAF IODOPROPYNYL BUTYLCARBAMATE KAOLIN FRANKINCENSE DIHYDROXYALUMINUM AMINOACETATE PROPYLENE GLYCOL TARTARIC ACID TITANIUM DIOXIDE ALOE VERA LEAF SODIUM POLYACRYLATE (2500000 MW) POLYACRYLIC ACID (450000 MW) POLYSORBATE 80
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
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
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.
Questions
A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.Questions 1-866-682-4639
Storage and handling
Information about safe storage and handling of the drug product.Other Information ■ store at 20-25°C (68-77°F) ■ store in a cool dry place away from direct sunlight
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. When using this product ■ use only as directed ■ avoid contact with the eyes or on mucous membranes ■ do not apply to wounds or damaged skin ■ do not apply to irritated skin or if excessive irritation develops ■ do not bandage tightly or use with heating pad or device Stop use and ask a doctor if ■ you experience pain, swelling or blistering of the skin ■ condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days ■ arthritic pain persists for more than 10 days, or redness is present 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