Relief Flex
Menthol · Patch · Topical
Active ingredient
Active ingredient(s) Menthol 4.0%
Purpose
Purpose Topical analgesic
Uses
Use(s) ■ temporarily relieves pain associated with minor: muscle aches joint pain backache strains and sprains
Warnings
Warnings ■ For external use only ■ Do not use on wounds or damaged skin with a heating pad if you are allergic to menthol or any of the ingredients in this product ■ When using this product avoid contact with eyes or mucous membranes do not bandage tightly use only as directed keep away from excessive heat ■ Stop use and ask a doctor if rash occurs ■ Keep out of reach of children , If product is swallowed, get medical help or contact a Poison Control Center right away.
Keep out of reach of children
■ Keep out of reach of children , If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions ■ adults and children 12 years and older: apply to affected area not more than 1 to 2 times daily rub in thoroughly until absorbed ■ children under 12 years of age: ask a doctor
Inactive ingredients
Inactive ingredients Mineral Oil, Hydrogenated Dicyclopentadiene/Isopentene/Isoprene/Styrene Copolymer, Hydrogenated Styrene/Butadiene Copolymer, Silicate, Ginger, Soil mineral, Styrene Copolymer, Hydrogenated Styrene, Butadiene/Isoprene Copolymer, 1,2-Hexandiol, Lavender Oil, Chamomile Oil, Nitric oxide, Cordyceps Sinensis Extract, Gardenia, MSM
Questions?
Questions ■ www.kbeone.com
Label text from the FDA structured product label by Beone Co., Ltd. (revised Feb 3, 2026). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Menthol in 1 product
Relief Flex NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 87379-010 | Menthol 4 g/100g Patch | Beone Co., Ltd. | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Relief Flex used for?
Use(s) ■ temporarily relieves pain associated with minor: muscle aches joint pain backache strains and sprains
Who makes Relief Flex?
Relief Flex is listed by 1 labeler in the FDA NDC directory, including Beone Co., Ltd..