Relief Flex

Manufacturer
Beone Co., Ltd.
Effective date
2026-02-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:36:20

Label at a glance#

ProductRelief Flex
Active ingredientMENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient(s)

Menthol 4.0%

OTC - PURPOSE SECTION

Purpose

Topical analgesic

INDICATIONS & USAGE SECTION

Use(s)

■ temporarily relieves pain associated with minor:

muscle aches

joint pain

backache

strains and sprains

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ Keep out of reach of children, If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton ImageCarton Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
853276menthol 4 % Medicated PatchPSN1
853276menthol 0.04 MG/MG Medicated PatchSCD1
853276menthol 4 % Medicated PatchSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
46e64ad7-7dca-4816-a2a4-8cdff2136105Product name220240828

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87379-010-01Relief Flex35 g in 1 CARTONPATCH351

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87379-01087379-010-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Relief FlexMENTHOLBeone Co., Ltd.49e6f0ef-78fb-26fe-e063-6294a90a66552026-02-03WarningsExact identifier
ndc (package): 87379-010-01
ndc (product): 87379-010
ndc11 (package): 87379001001
spl id: 49e6f0ef-78fc-26fe-e063-6294a90a6655
spl set id: 49e6f0ef-78fb-26fe-e063-6294a90a6655

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.