ACTIVON ULTRA STRENGTH ARTHRITIS- menthol, unspecified form stick 
Family First Pharmaceuticals, Inc.

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.

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ActivOn® Ultra Strength Arthritis

Drug Facts

Active Ingredient

Menthol 5.138%

Purpose

Topical Analgesic

Uses

Warnings

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.

Directions

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

NEW STRONGEST

ACTIVON® ARTHRITIS

ACTIVON®
Topical Analgesic

ULTRA
STRENGTH
ARTHRITIS

Powerful Pain Relief
for Arthritis &
Joint & Muscle Pain

No-Mess

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

PRINCIPAL DISPLAY PANEL - 57 g Canister Carton
ACTIVON ULTRA STRENGTH ARTHRITIS 
menthol, unspecified form stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51068-507
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A) Menthol, Unspecified Form0.05138 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
diazolidinyl urea (UNII: H5RIZ3MPW4)  
alcohol (UNII: 3K9958V90M)  
iodopropynyl butylcarbamate (UNII: 603P14DHEB)  
menthyl lactate, (-)- (UNII: 2BF9E65L7I)  
propylene glycol (UNII: 6DC9Q167V3)  
sodium stearate (UNII: QU7E2XA9TG)  
steareth-21 (UNII: 53J3F32P58)  
Edetate Sodium (UNII: MP1J8420LU)  
trolamine (UNII: 9O3K93S3TK)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51068-507-011 in 1 CARTON02/15/2017
157 g in 1 CANISTER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34802/15/2017
Labeler - Family First Pharmaceuticals, Inc. (832435809)
Establishment
NameAddressID/FEIBusiness Operations
RNA Pharma, LLC079103999MANUFACTURE(51068-507)

Revised: 2/2017
Document Id: 315fd1be-ae83-460e-96ac-e8117ded1dd7
Set id: 09d6b5a1-9223-4b60-b92d-7883a434a13e
Version: 1
Effective Time: 20170221
 
Family First Pharmaceuticals, Inc.