Acuplus Pain Relief Cream
FDA Label NDC 72037-135
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Innovations For Wellness, Llc for the product Acuplus Pain Relief (NDC 72037-135). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredient:, purpose, uses:, warnings:, when using this product:, stop use and ask doctor if:, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient:
Menthol 3.50%
Purpose
Topical Analgesic
Uses:
Temporary relief from minor aches and pains of sore muscles & Joints associated with arthritis, si ple backache, strains, bruises & sprains.
Warnings:
Use only as directed.
When Using This Product:
Avoid contact with the eyes or mucous membranes.
Stop Use And Ask Doctor If:
Condition worsens, or if symptoms persist for more than 7 days.
Directions:
Adults and children 2 years of age and older: Apply to affected area not more than three to four times daily.
Children under 2 years of age: consult a physician. Store at room temperature.
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.
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