RELIEF FLEX- menthol patch

Relief Flex by

Drug Labeling and Warnings

Relief Flex by is a Otc medication manufactured, distributed, or labeled by Beone Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient(s)

Menthol 4.0%

PURPOSE

Purpose

Topical analgesic

INDICATIONS & USAGE

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.

DOSAGE & ADMINISTRATION

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

OTHER SAFETY INFORMATION

Other Information

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

QUESTIONS

Questions

■ www.kbeone.com

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RELIEF FLEX 
menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87379-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
STYRENE (UNII: 44LJ2U959V)
OPHIOCORDYCEPS SINENSIS (UNII: 8Q1GYP08KU)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
LAVENDER OIL (UNII: ZBP1YXW0H8)
CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
GINGER (UNII: C5529G5JPQ)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
NITRIC OXIDE (UNII: 31C4KY9ESH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87379-010-01	35 g in 1 CARTON; Type 0: Not a Combination Product	02/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/01/2026

Labeler - Beone Co., Ltd. (695578618)

Establishment
Name	Address	ID/FEI	Business Operations
Beone Co., Ltd.		695578618	manufacture(87379-010)