Lanlijen, Menthol Pain Relief, 3fl.oz/89ml, Gel

Manufacturer
Jiangsu Chaben Medical Healthcare Technology Co.,Ltd | Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
Effective date
2022-12-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:52:31

Label at a glance#

ProductLanlijen Menthol Pain Relief
Active ingredientMENTHOL
Label structure17 sections

Indications and uses

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

Dosage and administration

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

Storage and handling

• Store in a cool dry place

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 4.0% w/w ...... Purpose: Topical Analgesic

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

OTC - ASK DOCTOR SECTION

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

OTC - STOP USE SECTION

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

OTC - WHEN USING SECTION

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

OTC - DO NOT USE SECTION

• 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 SECTION

• Store in a cool dry place

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

OTC - ASK DOCTOR/PHARMACIST SECTION

Children under 12 years of age, Consult physician

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Container PackageContainer PackageBox LabelingBox Labeling

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
415974menthol 4 % Topical GelPSN1
415974menthol 0.04 MG/MG Topical GelSCD1
415974menthol 4 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83050-232-302024-01-30C16284748780-11030e365-5780-111a-e063-dadaa90a10e2Lanlijen, Menthol Pain Relief, 3fl.oz/89ml, Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83050-232-30Lanlijen Menthol Pain Relief90 g in 1 BOTTLEGEL901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83050-232LANLIJEN MENTHOL PAIN RELIEF (MENTHOL) GEL [JIANGSU CHABEN MEDICAL HEALTHCARE TECHNOLOGY CO.,LTD]1Legacy NDC, 1 package rows20221217_efb48b37-6e1a-3d32-e053-2995a90aafaa.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83050-23283050-232-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
efb48b37-6e1b-3d32-e053-2995a90aafaaefb48b37-6e1a-3d32-e053-2995a90aafaa2022-12-13WarningsExact identifier
spl id: efb48b37-6e1b-3d32-e053-2995a90aafaa
spl set id: efb48b37-6e1a-3d32-e053-2995a90aafaa

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.