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| Product NDC Code | 79481-9966 | ||||
|---|---|---|---|---|---|
| Drug Name | Meijer cold therapy pain relieving |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | PATCH | ||||
| RxCUI drug identifier | 420222 | ||||
| Application Number | M017 | ||||
| Labeler Name | Meijer Inc | ||||
| 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.Active Ingredient Menthol 5%
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 Directions Adults and children 12 years of age and over: Clean and dry affected area, free of lotions, ointments, and creams. Carefully remove backing from patch. Apply sticky side of patch to affected area. Do not use more than one patch in an 8 hour period. Repeat as necessary. Maximum 3 patches per day. Discard patch after single use. Children under 12 years of age: consult a physician.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients aloe vera extract, arnica montana extract, boswellia carterii resin extract, carboxymethylcellulose sodium, dihydroxyaluminum aminoacetate, ethylhexylglycerin, glycerin, green tea extract, iodopropynyl butylcarbamate, kaolin, mineral oil, petrolatum, phenoxyethanol, polyacrylic acid, polysorbate 80, povidone, propylene glycol, sodium polyacrylate, tartaric acid, titanium dioxide, 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.Use Use For temporary relief of minor aches and pains of muscles and joints: arthritis, simple backache, bursitis, tendonitis, muscle strains, muscle sprains, bruises, and cramps.
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.Meijer Cold Therapy Pain Relieving Menthol DIHYDROXYALUMINUM AMINOACETATE PROPYLENE GLYCOL BOSWELLIA SERRATA RESIN OIL POLYACRYLIC ACID (8000 MW) WATER MINERAL OIL POVIDONE PHENOXYETHANOL KAOLIN TITANIUM DIOXIDE PETROLATUM MENTHOL MENTHOL GLYCERIN CARBOXYMETHYLCELLULOSE SODIUM TARTARIC ACID IODOPROPYNYL BUTYLCARBAMATE ETHYLHEXYLGLYCERIN POLYSORBATE 80 ALOE VERA LEAF ARNICA MONTANA FLOWER SODIUM POLYACRYLATE (8000 MW) GREEN TEA LEAF
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.Pack
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 Keep out of reach of children. Do not use on infants. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) 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, not to exceed 86 F (30C)
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 Consult a doctor if Stop use and consult a doctor if ■ Condition worsens ■ Redness is present ■ Irritation develops ■ Symptoms persist for more than 7 days or clear up and occur again within a few days ■ You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.
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 When using this product ■ Use only as directed ■Rare cases of serious burns have been reported with products of this type ■Don't bandage tightly or use with heating pad ■Avoid contact with eyes and mucous membranes ■Don't apply to wounds or damaged skin ■Do not use at the same time as other topical analgesics.
Pregnancy or breast feeding
Pregnancy or Breast feedingIf pregnant or breastfeeding 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 When using this product When using this product ■ Use only as directed ■Rare cases of serious burns have been reported with products of this type ■Don't bandage tightly or use with heating pad ■Avoid contact with eyes and mucous membranes ■Don't apply to wounds or damaged skin ■Do not use at the same time as other topical analgesics. Stop use and Consult a doctor if Stop use and consult a doctor if ■ Condition worsens ■ Redness is present ■ Irritation develops ■ Symptoms persist for more than 7 days or clear up and occur again within a few days ■ You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied. If pregnant or breastfeeding ask a health professional before use Keep out of reach of children Keep out of reach of children. Do not use on infants. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) 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