LANLIJEN MENTHOL PAIN RELIEF- menthol patch

Lanlijen Menthol Pain Relief by

Drug Labeling and Warnings

Lanlijen Menthol Pain Relief by is a Otc medication manufactured, distributed, or labeled by Jiangsu Chaben Medical Healthcare Technology Co.,Ltd, Shanghai Chuangshi Medical Technology (Group) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Menthol 5.0% w/w ...... Purpose: Topical Analgesic

Purpose

Topical Analgesic

Uses

Temporary relief from minor aches and pains of sore muscles and joints associated with arthritic, backache, strains and sprains

Warnings

For external use only

Flammable, Keep away from excessive heat or open flame

Ask a doctor before use if you have Sensitive Skin

Stop use and ask a doctor if burning discomfort or excessive skin irritation develops, conditions worsen, or symptoms persist for more than 7 days, or clear up and reoccur within a few days

ASK DOCTOR

Ask a doctor before use if you have Sensitive Skin

Stop use and ask a doctor if burning discomfort or excessive skin irritation develops, conditions worsen, or symptoms persist for more than 7 days, or clear up and reoccur within a few days

STOP USE

Stop use and ask a doctor if burning discomfort or excessive skin irritation develops, conditions worsen, or symptoms persist for more than 7 days, or clear up and reoccur within a few days

When using this product

Avoid contact with eyes or mucous membranes Do not use with other creams, sprays, ointments, or liniments Do not apply to wounds or damaged skin Do not apply to irritated skin or if excessive irritation develops Do not use with heating pad or device Store in a cool dry place Do not bandage Use only as directed Wash hands after use with cool water.

DO NOT USE

Do not use with other creams, sprays, ointments, or liniments Do not apply to wounds or damaged skin Do not apply to irritated skin or if excessive irritation develops Do not use with heating pad or device

STORAGE AND HANDLING

Store in a cool dry place

If pregnant or breast-feeding

Ask a health professional before use

Keep out of reach of children

If accidentally ingested, get medical help or contact a Poison Control Center immediately

Directions

Adults and children 12 years of age and older, Carefully remove remaining film while pressing patch to skin and leave in place for up to 8 hours. Use on affected areas not more than 4 times daily. Wash hands with cool water after use. Clean and dry afected areas, partially peel back protective film and apply exposed patch to site of pain.

Children under 12 years of age, Consult physician

ASK DOCTOR/PHARMACIST

Children under 12 years of age, Consult physician

Inactive Ingredients

Aloe barbadensis leaf extract, Arnica montana flower extract, Benzalkonium chloride, Boswellia carterii resin extract, Camellia sinensis leaf extract, Carboxymethylcellulose sodium, Dihydroxyaluminum aminoacetate, Edetate disodium, Glycerin, Kaolin, Lauralkonium chloride, L-Tartaric acid, Mineral oil, Petrolatum, PVP, Polyacrylic acid, Polysorbate 80, Propylene glycol, Sodium polyacrylate, Titanium dioxide, Water

Questions or Comments

86-513-89072216

E-mail:info@lanlijen.com
www.lanlijen.com
Tel:86-513-89072216

OTHER SAFETY INFORMATION

No Animal Testing, No NSAIDs, lbuprofen, Aspirin or Salicylate

Package label. Principal display panel

INGREDIENTS AND APPEARANCE

LANLIJEN MENTHOL PAIN RELIEF 
menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83050-251
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.05 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)
EDETATE DISODIUM (UNII: 7FLD91C86K)
KAOLIN (UNII: 24H4NWX5CO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
GLYCERIN (UNII: PDC6A3C0OX)
FRANKINCENSE (UNII: R9XLF1R1WM)
BENZODODECINIUM CHLORIDE (UNII: Y5A751G47H)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
TARTARIC ACID (UNII: W4888I119H)
MINERAL OIL (UNII: T5L8T28FGP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POVIDONE K90 (UNII: RDH86HJV5Z)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83050-251-05	5 in 1 BOX	12/15/2022
1	NDC: 83050-251-01	9 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 not final	part348	12/15/2022

Labeler - Jiangsu Chaben Medical Healthcare Technology Co.,Ltd (615936219)

Registrant - Jiangsu Chaben Medical Healthcare Technology Co.,Ltd (615936219)

Establishment
Name	Address	ID/FEI	Business Operations
Shanghai Chuangshi Medical Technology (Group) Co., Ltd.		546872672	manufacture(83050-251)