LANLIJEN MENTHOL PAIN RELIEF- menthol gel

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 4.0% 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 apply to wounds or damaged skin Do not apply to irritated skin or if excessive irritation develops Do not use with other creams, sprays, ointments, or liniments 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 apply to wounds or damaged skin Do not apply to irritated skin or if excessive irritation develops Do not use with other creams, sprays, ointments, or liniments 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, Rub a thin film over affected areas not more 4 times daily; massage not necessary

Children under 12 years of age, Consult physician

ASK DOCTOR/PHARMACIST

Children under 12 years of age, Consult physician

Inactive Ingredients

Alcohol, Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Boswellia Carterii Resin Extract, Camellia Sinensis Leaf Extract, Camphor, Carbomer, FD&C Blue 1, FD&C Yellow 5, Glycerin, llex Paraguariensis Leaf Extract, Isopropyl Myristate, Silica, Triethanolamine, Vitamin E, 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 gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83050-232
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
WATER (UNII: 059QF0KO0R)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
GLYCERIN (UNII: PDC6A3C0OX)
FRANKINCENSE (UNII: R9XLF1R1WM)
ALCOHOL (UNII: 3K9958V90M)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
TROLAMINE (UNII: 9O3K93S3TK)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83050-232-30	90 g in 1 BOTTLE; Type 0: Not a Combination Product	12/15/2022

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(83050-232)