Quick answers
- What is Borneol, camphor (synthetic) and menthol used for?
- The Drug Facts label of Sumifun Knee Relieving Patch (Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd) lists these uses: Temporarily relieves muscle soreness and minor joint pains in the knees, back,neck,hips,shoulders,elbows.
- Do I need a prescription for Borneol, camphor (synthetic) and menthol?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Borneol, camphor (synthetic) and menthol been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Sumifun Knee Relieving Patch · Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
Borneol 1.2 g/1001 · Camphor (synthetic) 1.5 g/1001 · Menthol 1 g/1001, patch (topical)
Active ingredient
Borneol 1.2% Camphor 1.5% Menthol 1.0%
Purpose
Topical Anaglesic
Uses
Temporarily relieves muscle soreness and minor joint pains in the 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 Ask Doctor Children under age of 12 When Using ·use only as directed ·avoid contact with the eyes, mucous membranes, or rashes ·do not bandage tightly Stop Use ·skin reactions such as redness,swelling,blistering or other discomfort occur ·symptoms persist for more than 7 days Keep Out Of Reach Of Children
Keep out of reach of children
Directions
·Clean and dry the affected area. ·Peel off the large protective film to reveal a small film on the reddish brown patch. ·Partially peel back the protective film and apply the exposed part of the patch to the the site of pain. ·Carefully remove remaining film while pressing the patch firmly on the skin. ·Remove patch from the skin after at most 8-hour application.
Inactive ingredients
Dried ginger, Saffron, Wormwood, Mugwort oil, Osmanthus flower oil, Eucalyptus leaf oil,Cinnamon
Questions?
sumifunofficial@gmail.com
— FDA label of Sumifun Knee Relieving Patch, Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd, effective January 6, 2024. See the official label on DailyMed →
Mqforu Pain Patch · Zhengzhou Miaoqi Medical Technology Co., Ltd.
Borneol 1.2 g/1001 · Camphor (synthetic) 1.5 g/1001 · Menthol 2 g/1001, patch (topical)
Active ingredient
Menthol 2.0% Borneol 1.2% Camphor 1.5%
Purpose
Topical Analgesic
Uses
Target User: for sub healthy people with discomfort caused by neck, shoulder,waist and leg.
Warnings
For external use only.
Do not use
When using this product
- use only as directed
- do not bandage tighty or use with a heating pad
- avoid contact with eyes and mucous membranes
- do not apply to wounds or damaged, broken or imitated skin
- do not use at the same time as other topical analgesics Ask Doctor Stop use and ask doctor if:
- rash, itching or excessive skin irritation develops
- condition worsens
- symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
If pregnant or breastfeeding
ask a health professional before use
Keep out of reach of children
- If swallowed, get medical help or contact a Poison Control Center right away When Using
When using this product
- use only as directed
- do not bandage tighty or use with a heating pad
- avoid contact with eyes and mucous membranes
- do not apply to wounds or damaged, broken or imitated skin
- do not use at the same time as other topical analgesics Stop Use Stop use and ask doctor if:
- rash, itching or excessive skin irritation develops
- condition worsens
- symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
If pregnant or breastfeeding
ask a health professional before use
Keep out of reach of children
- If swallowed, get medical help or contact a Poison Control Center right away Keep Out Of Reach Of Children
Keep out of reach of children
Directions
adults and children over 12 years:
- clean and dry the affected area
- remove backing from patch and apply patch to affected area
- use 1 patch per knee for 8 to 12 hours, once per day children 12 years or younger: ask a doctor
Inactive ingredients
Radix Angelicae Pubescentis, Drynaria Rhizome, Myrrh, Frankincense, Elderberry, Safflower, Angelicae, and Trachlospermi Caulis Et Folium
Questions?
Questions or comments? Email: mqforu86@gmail.com
— FDA label of Mqforu Pain Patch, Zhengzhou Miaoqi Medical Technology Co., Ltd., effective April 22, 2025. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Borneol 1.2 g/1001 · Camphor (synthetic) 1.5 g/1001 · Menthol 1 g/1001 · patch (topical) · 2 products
Borneol 1.2 g/1001 · Camphor (synthetic) 1.5 g/1001 · Menthol 2 g/1001 · patch (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Mqforu Pain Patch | Zhengzhou Miaoqi Medical Technology Co., Ltd. | DailyMed |
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd2 products
- Zhengzhou Miaoqi Medical Technology Co., Ltd.1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youA pharmacist can answer questions about this label
- Latest FDA drug recallsPrescription and over-the-counter, newest first
- All over-the-counter medicinesSearch by ingredient, brand or Spanish name
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.