CORISIN ARTHRITIS PAIN RELIEF- capsaicin, menthol gel

CORISIN ARTHRITIS PAIN RELIEF by

Drug Labeling and Warnings

CORISIN ARTHRITIS PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

CORISIN ARTHRITIS PAIN RELIEF 
capsaicin, menthol gel

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
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 Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/21/2014

Labeler - Pure Source, LLC (080354456)

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