CORISIN ARTHRITIS PAIN RELIEF GEL

Active ingredient

Capsaicin 0.025% Menthol 10%

Purpose

Topical Analgesic

Uses

For temporary relief of minor aches and pains associated with

Simple back ache
Arthritis
Sprains
Cramps

For external use only

When using this product

Read inside of carton before using
Use only as directed
Do not bandage tightly or cover treated areas
Do not use with heating pad
Avoid contact with eyes and mucous membranes
Do not apply to wounds or damaged, broken or irritated skin
A mild burning sensation may occur. If severe burning sensation occurs, discontinue use immediately
If symptoms persist for more than seven days, discontinue and consult physician

Keep out of reach of children

If swallowed, consult physician

If pregnant or breast feeding

contact physician prior to use.

Directions

Adult and children over 18 years:

Apply directly to effected area. Repeat as necessary, but do not use more than 3-4 times daily.

Other Ingredients

Allantoin, Aloe Barbadensis (Aloe Vera) Juice, Aqua (Deionized Water), Carbomer, DMDM Hydrantoin, Glycerin, Methyl Paraben, Polysorbate-20, Propyl Paraben, Glycol, Triethanolamine.

CORISIN ARTHRITIS PAIN RELIEF GEL 1oz/28.3g (65121-498-01)

CORISIN ARTHRITIS PAIN RELIEF
capsaicin, menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:65121-498
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.025 g in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
ALLANTOIN (UNII: 344S277G0Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
DMDM HYDANTOIN (UNII: BYR0546TOW)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:65121-498-01	1 in 1 BOX	02/09/2017
1		28.3 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	04/21/2014

Labeler - Pure Source, LLC (080354456)

Name	Address	ID/FEI	Business Operations
Establishment
Pure Source, LLC		080354456	manufacture(65121-498)