FDA Label for Arthritis Relief
View Indications, Usage & Precautions
Arthritis Relief Product Label
The following document was submitted to the FDA by the labeler of this product Newmarket Health Products Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
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:
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