Drug Facts

Active Ingredient	Purpose
Histamine Dihydrochloride 0.028%	Topical Analgesic
Menthol 4.574%	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 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 medical 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

diazoldinyl urea, ethyl alcohol, iodopropynyl butlylcarbamate, menthyl lactate, propylene glycol, sodium stearate, steareth-21, tetrasodium EDTA, triethenolamine, water

Questions ?

call 1-800-379-8870, Weekdays 9AM to 5PM EST or visit us online at activ-on.com

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

PRINCIPAL DISPLAY PANEL - 57 g Carton

NEW
STRONGEST
ACTIVON® ARTHRITIS

ACTIVON®
Topical Analgesic

ULTRA
STRENGTH
ARTHRITIS

Powerful Pain Relief
for Arthritis & Joint & Muscle Pain

No-Mess

NDC 51068-501-01
NET WT 2 OZ (57 g)

ACTIVON ULTRA STRENGTH ARTHRITIS
menthol and histamine dihydrochloride stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51068-501
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Menthol, unspecified form (UNII: L7T10EIP3A) (Menthol, unspecified form - UNII:L7T10EIP3A)	Menthol, unspecified form	0.04574 g in 1 g
Histamine Dihydrochloride (UNII: 3POA0Q644U) (Histamine - UNII:820484N8I3)	Histamine Dihydrochloride	0.00028 g in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description
Packaging
1	NDC:51068-501-01	1 in 1 CARTON
1		57 g in 1 CANISTER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH NOT FINAL	part348	09/01/2011

Labeler - Family First Pharmaceuticals, Inc. (832435809)

Name	Address	ID/FEI	Business Operations
Establishment
RNA Pharma, LLC		079103999	MANUFACTURE(51068-501)

ACTIVON® Topical Analgesic ULTRA STRENGTH ARTHRITIS