ARTHRITIS PAIN RELIEF- capsaicin 0.15 liquid

Arthritis Pain Relief by

Drug Labeling and Warnings

Arthritis Pain Relief by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Capsaicin 0.15%

Purpose

Topical analgesic

Uses

Temporarily relieves minor pain associated with:

• arthritis
• simple backache
• muscle strains
• muscle sprains
• bruises
• cramps

Warnings

​For external use only

When using this product

• Use only as directed
• Do not bandage tightly
• Do not use with a heating pad
• Avoid contact with eyes and mucous membranes
• Do not apply to wounds, damaged, broken or irritated skin
• A transient burning sensation may occur upon application but generally disappears in several days
• If severe burning sensation occurs, discontinue use immediately and read packate insert for importan information
• Do not expose the area treated with product to hear or direct sunlight
• Avoid taking a bath or shower within 1 hour before or after applying

Stop use and ask a doctor if

• Condition worsens
• Redness is present
• Irritation develops
• Symptoms persist for more than 7 days or clear up and occur again within a few days

Flammable

keep away form fire or flame

If pregnant or breast-feeding,

ask a healthcare professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison COntrol Center right away.

Directions

​​Adults and children over 18 years:

• Apply to affected area
• Massage into painful area until thoroughly absorbed
• Repeat as necessary, but no more than 3 to 4 times daily
• ​IF MEDICINE COMES IN CONTACT WITH HANDS, WASH WITH SOAP AND WATER

​

Children 18 years or younger: ask a doctor

Inactive ingredients

Carbomer, Glycerin, Propylene Glycol, SD Alcohol 40-2 (35%), Triethanolamine, Water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARTHRITIS PAIN RELIEF 
capsaicin 0.15 liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-237
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	.15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALCOHOL (UNII: 3K9958V90M)
TROMETHAMINE (UNII: 023C2WHX2V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-237-01	1 in 1 CARTON	11/11/2014
1		30 mL in 1 BOTTLE, WITH APPLICATOR; 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	11/11/2014

Labeler - CVS (062312574)

Registrant - Product Quest Mfg, LLC (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	manufacture(59779-237) , label(59779-237)