Pain Relief Patch by QUEST USA CORP. PAIN RELIEF PATCH patch

Pain Relief Patch by

Drug Labeling and Warnings

Pain Relief Patch by is a Otc medication manufactured, distributed, or labeled by QUEST USA CORP.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

CAMPHOR (SYNTHETIC) 80mg
MENTHOL 24mg
NONIVAMIDE 16mg

Purpose

Topical analgesic

Use

For temporary relief of pains

Warnings

For external use only

Do not use

·Do not get into eyes or on mucous membranes
·Do not apply to wounds, damaged or irritated skin
·Do not bandage or cover with any type of wrap except clothing
·Do not use with a heating pad or apply external heat
·Do not use 1 hour prior to bathing or within 30 minutes after bathing

When Using

When using this product·Use only as directed

Stop Use

Stop use and ask a doctor if
·Condition worsens
·Severe skin irritation occurs
·Pain persists for more than 7 days
·Symptoms clear up and occur again within a few days

Ask Doctor

If pregnant or breast-feeding, or if you have sensitive skin, ask a healthcare professional before use.
Children under 12 years, consult doctor before use

Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

Directions
·Adults and children 12 years and over apply to affected area; change patch 1 to 2 times daily
·Children under 12 years, consult doctor before use
How to apply:
·Clean and dry affected area
·Cut open pouch and remove patch
·Remove protective film and apply directly to area of pain
·Apply to affected area not more than 3 times daily
·Wash hands with soap after applying patch
·Reseal pouch containing unused patches

Other information

Other information
This product may cause allergic reaction on some individuals.Store in cool dry place away from direct sunlight.

Inactive ingredients

Inactive ingredients
Aluminum Glycinate, Ethylhexylglycerin, Eucalyptus Oil, Glycerin, Kaolin, Mentha Oil, Phenoxyethanol, Polyvinylpyrrolidone,Propylene Glycol, Sodium Carboxymethylcellulose, Sodium Polyacrylate, Sorbitol Solution, Tartaric Acid, Water

Questions

Questions?

1-800-910-6874

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAIN RELIEF PATCH 
pain relief patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78691-141
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	80 mg  in 100
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	24 mg  in 100
NONIVAMIDE (UNII: S846B891OR) (NONIVAMIDE - UNII:S846B891OR)	NONIVAMIDE	16 mg  in 100

Inactive Ingredients
Ingredient Name	Strength
EUCALYPTUS OIL (UNII: 2R04ONI662)
PEPPERMINT OIL (UNII: AV092KU4JH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM ACRYLATE (UNII: 7C98FKB43H)
WATER (UNII: 059QF0KO0R)
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
KAOLIN (UNII: 24H4NWX5CO)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
SORBITOL SOLUTION (UNII: 8KW3E207O2)
TARTARIC ACID (UNII: W4888I119H)
POVIDONE (UNII: FZ989GH94E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78691-141-01	5 in 1 BOX; Type 0: Not a Combination Product	06/14/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	06/14/2024

Labeler - QUEST USA CORP. (079869689)