FDA.reportPublic FDA data

87721-006-01 EAYONYUM KNEE PAIN RELIEVING MENTHOL PATCHES, 100 COUNT

Manufacturer
Wuhan Ruihengjie Technology Co., Ltd.
Effective date
2026-08-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-02 00:03:31

Label at a glance#

ProductEAYONYUM KNEE PAIN RELIEVING
Active ingredientMENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient
Menthol 2%
Purpose
Topical analgesic

OTC - PURPOSE SECTION

Uses
Temporarily relieves minor aches and pains of muscles and joints associated with
simple backache
arthnitis
strains
bruises
sprains

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Contral Center right
away.

WARNINGS SECTION

Warnings For external use only.
Do not use
on wounds or damnaged skin
with a heating pad
on inritated or infected skin
When using this product
use only as directed
avoid contact with eyes and mucous membrares do not bandage lightly
Stop use and ask a doctor if
conditions worsens
symptoms clear up and occur again within a tew days
symptoms persist far more than 7 days
excessive irritation develops
If pregnant or breast-leeding, ask a health professional before use

DOSAGE & ADMINISTRATION SECTION

remove protective film and apply 1 patch to the affected area
remove after no more than 8 hours
use up to 3 times daily

INDICATIONS & USAGE SECTION

Directions
Adults and children 12 years and older
clean and dry the affected area
remove protective film and apply 1 patch to the affected area
remove after no more than 8 hours
use up to 3 times daily

INACTIVE INGREDIENT SECTION

Carthamus Tinctorius (Safflower) Flower Extract

Panax Notoginseng Root Extract

Zanthoxylum Bungeanum Fruit Extract

Spatholobus Suberectus Stem Extract

Artemisia Argyi Leaf Oil

Turpentine Oil

Wintergreen Oil

Capsicum Oil

Borneol

Camphor

Menthol

Hot Melt Adhesive

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
87721-00687721-006-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
CARTHAMUS TINCTORIUS (SAFFLOWER) FLOWER4VBL71TY4YIACT
PANAX NOTOGINSENG ROOTGQX1C1175UIACT
ZANTHOXYLUM BUNGEANUM FRUIT3CIP16A418IACT
SPATHOLOBUS SUBERECTUS STEMN51VZ363BAIACT
ARTEMISIA ARGYI LEAF2JYC99Q0WZIACT
TURPENTINE OILC5H0QJ6V7FIACT
GAULTHERIA PROCUMBENS (WINTERGREEN) LEAF OILLAV5U5022YIACT
CAPSICUM OLEORESINUW86K581WYIACT
BORNEOLM89NIB437XIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT

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
EAYONYUM KNEE PAIN RELIEVINGMENTHOLWuhan Ruihengjie Technology Co., Ltd.5a45d19f-c753-71eb-e063-6294a90a48052026-08-30WarningsExact identifier
ndc (package): 87721-006-01
ndc (product): 87721-006
ndc11 (package): 87721000601
spl id: 5a45d19f-c754-71eb-e063-6294a90a4805
spl set id: 5a45d19f-c753-71eb-e063-6294a90a4805

Reported adverse events (FAERS/openFDA)#

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