AcuPlus Pain Relief
AcuPlus Pain Relief is an FDA drug label for the active ingredient MENTHOL manufactured by Innovations for Wellness, LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231105.
Generic: MENTHOL
Manufacturer: Innovations for Wellness, LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 72037-135
Application: M017
Effective: 20231105
Active Ingredients: Active Ingredient: Menthol 3.50% Purpose Topical Analgesic
Indications & Usage
Uses: Temporary relief from minor aches and pains of sore muscles & Joints associated with arthritis, si ple backache, strains, bruises & sprains.
Dosage & Administration
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:
Contraindications
Not available.
Warnings
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.
Adverse Reactions
Not available.
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