Arthritis Relief
FDA Label NDC 50972-300

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Newmarket Health Products Llc for the product Arthritis Relief (NDC 50972-300). 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 active ingredient, purpose, use, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Menthol 1.25%

Purpose

Topical Analgesic

Use

Temporarily relieves minor aches and pains of muscles and joints associated with:

  • simple backache
    • arthritis
      • strains
        • bruises
          • sprains

Warnings

For external use only

Do Not Use

  • on wounds or damaged skin

When Using This Product

  • avoid contact with eyes or mucous membranes
  • do not bandage tightly

Stop Use And Ask A Doctor If

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adult and children 12 years of age or older: Apply to affected area not more than 3 to 4 times daily.
  • Children under 12 years of age: Consult a physician.

Inactive Ingredients:

aloe vera gel, cetyl alcohol, cetyl esters (proprietary blend of esterfied fatty acids), cinnamon oil, eucalyptus oil, glyceryl stearate, grape seed oil, hypromellose, jojoba oil, peppermint oil, phenoxyethanol, potassium sorbate, purified water, sodium benzoate, squalane, stearic acid, stearyl alcohol, tea tree oil, vegetable glycerin, wintergreen oil.

Questions?

1-800-895-2108

Package Labeling:

Label2 (Label2)

Label2 (Label2)

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