Indications and uses
Temporary relief from minor aches and pains of sore muscles and joints associated with arthritic, backache, strains and sprains
Lanlijen, Menthol Pain Relief, 2.5fl.oz/74ml, Gel
- Manufacturer
- Jiangsu Chaben Medical Healthcare Technology Co.,Ltd | Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
- Effective date
- 2022-10-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:51:03
Label at a glance#
ProductLanlijen Menthol Pain Relief
Active ingredientMENTHOL
Label structure17 sections
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
Contacts and useful links#
Websitewww.lanlijen.com
www.lanlijen.com
www.lanlijen.comLabel contents#
Full prescribing information#
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 conditions worsen, or symptoms persist for more than 7 days, or clear up and reoccur
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have Sensitive Skin
Stop use and ask a doctor if conditions worsen, or symptoms persist for more than 7 days, or clear up and reoccur
OTC - STOP USE SECTION
Stop use and ask a doctor if conditions worsen, or symptoms persist for more than 7 days, or clear up and reoccur
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
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
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
OTC - ASK DOCTOR/PHARMACIST SECTION
Children under 12 years of age, Consult physician
Inactive Ingredients
Arnica Montana Flower Extract, Aloe Barbadensis Leaf Extract, Camellia Sinensis Leaf Extract, Boswellia Carterii Resin Extract, Water, Alcohol, llex Paraguariensis Leaf Extract, Triethanolamine, Carbomer, Camphor, Glycerin, Silica, Isopropyl Myristate, Vitamin E, FD&C Blue 1, FD&C Yellow 5
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
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 83050-231-25 | 2024-01-30 | C162847 | 48780-1 | 1030e364-faff-111a-e063-dadaa90a10e2 | Lanlijen, Menthol Pain Relief, 2.5fl.oz/74ml, Gel |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83050-231-25 | Lanlijen Menthol Pain Relief | 75 g in 1 BOTTLE | GEL | 75 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Lanlijen Menthol Pain Relief
- Menthol
- FD&C BLUE NO. 1
- POLYACRYLIC ACID (250000 MW)
- WATER
- CAMPHOR (SYNTHETIC)
- SILICON DIOXIDE
- ISOPROPYL MYRISTATE
- ILEX PARAGUARIENSIS LEAF
- .ALPHA.-TOCOPHEROL, D-
- ALOE VERA LEAF
- ARNICA MONTANA FLOWER
- GLYCERIN
- FRANKINCENSE
- ALCOHOL
- GREEN TEA LEAF
- TROLAMINE
- FD&C YELLOW NO. 5
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 83050-231 | 83050-231-25 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| eaebb908-8538-c323-e053-2995a90a04d8 | eaebb908-8537-c323-e053-2995a90a04d8 | 2022-10-18 | Warnings | eaebb908-8538-c323-e053-2995a90a04d8 eaebb908-8537-c323-e053-2995a90a04d8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.