MENTHOL OVERNIGHT PAIN RELIEF GEL-PATCH- menthol patch

Menthol Overnight Pain Relief Gel-Patch by

Drug Labeling and Warnings

Menthol Overnight Pain Relief Gel-Patch by is a Otc medication manufactured, distributed, or labeled by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Menthol 4% ...... Purpose: Topical analgesic

Purpose

Topical Analgesic

Uses

Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.

Warnings

For external use only

Do not use

■ on wounds or damaged skin

■ with a heating pad or device

■ with other ointments, creams, sprays, or liniments

■ if you are allergic to any ingredients of this product

When using this product

■ use only as directed

■ avoid contact with the eyes, mucous membranes or rashes

■ do not bandage tightly

Stop use and ask a doctor if

■ skin reactions such as redness, swelling, blistering or other discomfort occur

■ symptoms persist for more than 7 days

If pregnant or breast-feeding,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN.

If swallowed accidentally, get medical help or contact with Poison Control Center immediately.

Directions

Adult and Children above 12 years old:

■ Clean and dry the affected area.

■ Tear off the protective film and apply the exposed part of the patch to the affected area.

■ Carefully remove remaining film while pressing the patch firmly on the skin.

■ Remove patch from the skin after at most 8-hour application.

Children under age of 12: Consult a doctor

Inactive ingredients

Benzalkonium Chloride, Carboxymethylcellulose Sodium, Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Kaolin, Lauralkonium Chloride, Lavender Essential Oil, L-Tartaric Acid, Mineral Oil, Petrolatum, Polyacrylic Acid, Polysorbate 80, Propylene Glycol, PVP, Sodium Polyacrylate, Titanium Dioxide, Water

Questions or Comments:

sumifunofficial@gmail.com

Package label. Principal display panel

INGREDIENTS AND APPEARANCE

MENTHOL OVERNIGHT PAIN RELIEF GEL-PATCH 
menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83602-123
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.04 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
WATER (UNII: 059QF0KO0R)
LAURALKONIUM CHLORIDE (UNII: 07HUP5A29X)
LAVENDER OIL (UNII: ZBP1YXW0H8)
KAOLIN (UNII: 24H4NWX5CO)
TARTARIC ACID (UNII: W4888I119H)
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
MINERAL OIL (UNII: T5L8T28FGP)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PETROLATUM (UNII: 4T6H12BN9U)
POVIDONE K90 (UNII: RDH86HJV5Z)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83602-123-15	15 in 1 BOX	02/05/2024
1	NDC: 83602-123-01	5.5 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/05/2024

Labeler - Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. (418399704)

Registrant - Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. (418399704)