ACTIVON ULTRA STRENGTH ARTHRITIS- menthol, unspecified form stick

ActivOn Ultra Strength Arthritis by

Drug Labeling and Warnings

ActivOn Ultra Strength Arthritis by is a Otc medication manufactured, distributed, or labeled by Family First Pharmaceuticals, Inc., RNA Pharma, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active Ingredient

Menthol 5.138%

Purpose

Topical Analgesic

Uses

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

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

• 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

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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)

INGREDIENTS AND APPEARANCE

ACTIVON ULTRA STRENGTH ARTHRITIS 
menthol, unspecified form stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51068-507
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A)	Menthol, Unspecified Form	0.05138 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51068-507-01	1 in 1 CARTON	02/15/2017
1		57 g in 1 CANISTER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	02/15/2017

Labeler - Family First Pharmaceuticals, Inc. (832435809)

Establishment
Name	Address	ID/FEI	Business Operations
RNA Pharma, LLC		079103999	MANUFACTURE(51068-507)