Quick answers
- What is Borneol and camphor (synthetic) used for?
- The Drug Facts label of Mqupin Knee Patch (Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd) lists these uses: temporarily relieves minor pain associated with; arthritis; muscle strains; sprains; bruises; joint pain.
- Do I need a prescription for Borneol and camphor (synthetic)?
- 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 and camphor (synthetic) 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.
Mqupin Knee Patch · Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
Borneol 1.2 g/1001 · Camphor (synthetic) 1.5 g/1001, patch (topical)
Active ingredient
Borneol 1.2% Camphor 1.5%
Purpose
Topical Analgesic
Uses
temporarily relieves minor pain associated with:
- arthritis
- muscle strains
- sprains
- bruises
- joint pain
Warnings
For external use only. Ask Doctor children 12 years or younger When Using
- 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
- 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
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
Inactive ingredients
Dried ginger, saffron, Wormwood, mugwort oil, osmanthus flower oil, eucalyptus leaf oil, cinnamon.
Questions?
mqupin86@gmail.com
— FDA label of Mqupin Knee Patch, Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd, effective May 8, 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 · patch (topical) · 2 products
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., Ltd1 product
- 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.
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.