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Amp relief pain relief cream - Medication Information

Product NDC Code 82560-283
Drug Name

Amp relief pain relief cream

Type Brand
Active Ingredients
Menthol 80 mg/ml
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 727161
Application Number M017
Labeler Name COASTAL FORMULAS LLC
Packages
Package NDC Code Description
82560-283-00 3939.19 ml in 1 jug (82560-283-00)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Menthol 8.00% 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 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: Consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients: Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glycerin, Isopropyl Myristate, Methyl Salicylate, Paraffinum Liquidum, Phenoxyethanol, Polysorbate-80, SD-Alcohol 40B, Triethanolamine, FD& C Blue #1, FD&C Yellow #5

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 backache, arthritis, strains, bruises, and 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.
AMP RELIEF Pain Relief Cream MENTHOL ALOE VERA LEAF WATER ARNICA MONTANA FLOWER INDIAN FRANKINCENSE ETHYLHEXYLGLYCERIN EUCALYPTUS OIL GLYCERIN ISOPROPYL MYRISTATE METHYL SALICYLATE MINERAL OIL PHENOXYETHANOL POLYSORBATE 80 TROLAMINE FD&C BLUE NO. 1 FD&C YELLOW NO. 5 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: Label0

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 Flammable: Keep away from exessive heat or open flame.

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 damaged or broken 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.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? 1(888) 510-6289

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 rash or irritation develops and lasts condition worsens sysmptoms persist for more than 7 days clears up and occurs again within a few days

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 the eyes. Do not bandage tightly.

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: For external use only. Do not use on damaged or broken skin When using this product Avoid contact with the eyes. Do not bandage tightly. Stop use and ask a doctor if rash or irritation develops and lasts condition worsens sysmptoms persist for more than 7 days clears up and occurs again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

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