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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.

ActivOn® Ultra Strength Arthritis

Drug Facts

Active Ingredient

Menthol 5.138%


Topical Analgesic

  • For the temporary relief of minor aches and pains of muscles and joints associated with
    • simple backache
    • arthritis
    • strains
    • bruises
    • sprains


For external use only.

Do not use
  • 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

When using this product
  • avoid contact with eyes, wounds, mucous membranes, broken or irritated skin
  • do not share this product with anyone
  • do not bandage tightly

Stop use and ask a doctor if
  • 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

Other information

Keep away from heat. Store between 15° and 30° C (59° and 86° F).

Inactive Ingredients

diazolidinyl urea, ethyl alcohol, iodopropynyl butylcarbamate, menthyl lactate, propylene glycol, sodium stearate, steareth-21, tetrasodium EDTA, triethanolamine, water

Questions ?

call 1-800-379-8870, Weekdays 9AM to 5PM EST

Dist. by Family First Pharmaceuticals, Inc., Reno, NV 89502

PRINCIPAL DISPLAY PANEL - 57 g Canister Carton



Topical Analgesic


Powerful Pain Relief
for Arthritis &
Joint & Muscle Pain


NDC 51068-507-01
NET WT 2 OZ (57 g)

menthol, unspecified form stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51068-507
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol, Unspecified Form (Menthol, Unspecified Form) Menthol, Unspecified Form0.05138 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
diazolidinyl urea 
iodopropynyl butylcarbamate 
menthyl lactate, (-)- 
propylene glycol 
sodium stearate 
Edetate Sodium 
#Item CodePackage Description
1NDC:51068-507-011 CANISTER in 1 CARTON
157 g in 1 CANISTER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34802/15/2017
Labeler - Family First Pharmaceuticals, Inc. (832435809)
RNA Pharma, LLC079103999MANUFACTURE(51068-507)

Family First Pharmaceuticals, Inc.

← See all ActivOn Ultra Strength Arthritis brands

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.