Q HEALTH PAIN RELIEF- menthol liquid

Q Health Pain Relief by

Drug Labeling and Warnings

Q Health Pain Relief by is a Otc medication manufactured, distributed, or labeled by QCAN International Inc., Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Q Health Pain Relief Spray

Active Ingredient:

Menthol  8.00%

Purpose

External Analgesic

Directions:

Apply directly to affected area.  Do not use more than four times per day.

Uses:

For temporary relief of minor aches and pains associated with simple backache, arthritis, bruises and sprains.

Warnings:

• For external use only.
• Avoid contact with eyes.
• Do not bandage tightly.
  

Do not apply

on open wounds or damaged skin.

Discontinue use

If symptoms persist more than seven days, discontinue use and consult physician.

Keep out of reach of children.

If swallowed, consult physician.

If pregnant or breast feeding,

contact physician prior to use.

Other Ingredients:

Aqua (Deionized Water), Arnica Montana Extract, Boswella Serrata Extract, Bromelain, Chondroitin Sulfate, Citric Acid, Dimethyl Sulfone (MSM), Eucalyptus Globulus Oil, Glucosamine Sulfate, Glycrrhiza Glabra (Licorice) Extract, Ilex Paraguariensis (Yerba Mate) Leaf Extract, Magnesium Sulfate, Mentha Piperita (Peppermint) Oil, Methylisothiazolinone, Polysorbate-20, Polysorbate-80, Propylene Glycol, SD-Alcohol 40B.

PRINCIPAL DISPLAY PANEL

Q Health PAIN Relief Spray   Fast temporary relief of minor aches and pains   associated with simple backache arthritis, strains, bruises, sprains    Contains Magnesium and Glucosamine Chondroitin MSM  www.qcan.ca     4 FL OZ (120ML)   Manufactured for   QCAN INTERNATIONAL   1581 Crimson Cres.  Kingston ON, K7P 0J3   Canada.

Product Labels

INGREDIENTS AND APPEARANCE

Q HEALTH PAIN RELIEF 
menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54102-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	80 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA (UNII: O80TY208ZW)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
BROMELAINS (UNII: U182GP2CF3)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EUCALYPTUS OIL (UNII: 2R04ONI662)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
PEPPERMINT OIL (UNII: AV092KU4JH)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54102-000-04	1 in 1 CARTON	02/07/2017
1		120 mL 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	09/13/2012

Labeler - QCAN International Inc. (246834035)

Establishment
Name	Address	ID/FEI	Business Operations
Pure Source, LLC		080354456	manufacture(54102-000)