ActivOn Ultra Strength Arthritis
Medically reviewed on February 21, 2017
Dosage form: stick
Ingredients: Menthol, Unspecified Form 0.05138g in 1g
Labeler: Family First Pharmaceuticals, Inc.
NDC Code: 51068-507
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
- For the temporary relief of minor aches and pains of muscles and joints associated with
- simple backache
For external use only.
- otherwise than as directed
- if you are allergic to any ingredient in this product
- on a child under 12 years of age with arthritis-like conditions
- with a heating pad
- avoid contact with eyes, wounds, mucous membranes, broken or irritated skin
- do not share this product with anyone
- do not bandage tightly
- condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
- skin redness or excessive irritation of the skin develops
If pregnant or breast-feeding, ask a health professional before use.
Keep out of the reach of children. If swallowed, get mediacal help or contact a Poison Control Center right away.
- adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily.
- children under 12 years of age: ask a doctor
Keep away from heat. Store between 15° and 30° C (59° and 86° F).
diazolidinyl urea, ethyl alcohol, iodopropynyl butylcarbamate, menthyl lactate, propylene glycol, sodium stearate, steareth-21, tetrasodium EDTA, triethanolamine, water
call 1-800-379-8870, Weekdays 9AM to 5PM EST
Dist. by Family First Pharmaceuticals, Inc., Reno, NV 89502
|ACTIVON ULTRA STRENGTH ARTHRITIS
menthol, unspecified form stick
|Labeler - Family First Pharmaceuticals, Inc. (832435809)|
|RNA Pharma, LLC||079103999||MANUFACTURE(51068-507)|
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.