ARNIMAX Penetrating Pain Relief Gel
ARNIMAX Penetrating Pain Relief Gel is an FDA drug label for the active ingredient MENTHOL manufactured by WYNNPHARM INC. 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 20231110.
Generic: MENTHOL
Manufacturer: WYNNPHARM INC.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 35324-274
Application: M017
Effective: 20231110
Active Ingredients: Active Ingredient: Menthol 3.00% Purpose Topical Analgesic
Indications & Usage
Uses: For the temporary relief of minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains
Dosage & Administration
Directions Adults and children over 12 years: • Apply and massage a thin layer to affected area no more than 3 to 4 times daily. • Wash hands with soap and water after applying. Ask a doctor. Children under 12:
Contraindications
Not available.
Warnings
Warning For external use only. Do not use if allergic to any ingredients listed in this product. When using this product • Use only as direcred • Avoid contact with eyes and mucous membranes • Do not apply directly to wounds or broken skin • Do not bandage tightly or use a heating pad. Stop use and ask a doctor if • Condition worsens • Condition persists for more than 7 days or clears up and occurs again within a few days. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If swallowed, seek medical attention or contact a Poison Control Center right away.
Adverse Reactions
Not available.
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