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Acuplus pain relief - Medication Information

Product NDC Code 72037-135
Drug Name

Acuplus pain relief

Type Brand
Active Ingredients
Menthol 35 mg/ml
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 2000534
Application Number M017
Labeler Name Innovations for Wellness, LLC
Packages
Package NDC Code Description
72037-135-01 3785 ml in 1 jug (72037-135-01)
72037-135-02 59.14 ml in 1 jar (72037-135-02)
72037-135-04 236.56 ml in 1 jar (72037-135-04)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
​Active Ingredient: Menthol 3.50% ​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: ​Apply to affected area not more than three to four times daily. ​Adults and children 2 years of age and older: ​consult a physician. Store at room temperature. ​Children under 2 years of age:

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
​Other Ingredients: Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Carbomer, Cetyl Myristoleate, Ethylhexylglycerin, Glucosamine Sulfate, Glycyrrhiza Glabra (licorice) Root Extract, Ilex Paraguayensis (Yerba Mate') Extract, Isopropyl Alcohol, Magnesium Sulfate, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polysorbate-20, Pyridoxine HCl (Vitamin B6), Salix Alba (Willow) Bark Extract, Tetrasodium EDTA, Tocophyeryl Acetate (Vitamin E), Triethanolamine.

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 & Joints associated with arthritis, si ple backache, strains, bruises & 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.
AcuPlus Pain Relief MENTHOL ALOE VERA LEAF WATER ARNICA MONTANA FLOWER INDIAN FRANKINCENSE CARBOXYPOLYMETHYLENE CETYL MYRISTOLEATE ETHYLHEXYLGLYCERIN GLUCOSAMINE SULFATE LICORICE ILEX PARAGUARIENSIS WHOLE ISOPROPYL ALCOHOL MAGNESIUM SULFATE, UNSPECIFIED FORM TEA TREE OIL DIMETHYL SULFONE PHENOXYETHANOL POLYSORBATE 20 PYRIDOXINE HYDROCHLORIDE SALIX ALBA BARK EDETATE SODIUM .ALPHA.-TOCOPHEROL ACETATE TROLAMINE 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.
AcuPlus Pain Relief Cream 1 Gallon Label 1 Galon AcuPlus Pain Relief Cream 2oz Label 2oz AcuPlus Pain Relief Cream 4oz Label 4oz

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

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 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 Do not use with heating pad or device Wash hands after use with cool water.

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

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? ​Call: +1 (855) 9740909 - Made in USA

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 doctor if: Condition worsens, or if symptoms persist for more than 7 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 or mucous membranes.

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: Use only as directed. Keep out of reach of children For external use only. Keep away from excessive heat or flame. When using this product: Avoid contact with the 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 Do not use with heating pad or device Wash hands after use with cool water. Stop use and ask doctor if: Condition worsens, or if symptoms persist for more than 7 days.

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