Herbal Knee Patch

Manufacturer
Henan Kangdi Medical Devices Co., Ltd
Effective date
2026-02-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:37:24

Label at a glance#

ProductHerbal Knee Patch
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure13 sections

Dosage and administration

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

Storage and handling

store at room temperature, not to exceed 86°F (30°C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor(SYNTHETIC) 1.5%
Menthol 1%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

temporarily relieves minor pain associated with:
■arthritis

■muscle strains

■sprains

■bruises

■ joint pain

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use at the same time as other topical analgesics

When Using

OTC - WHEN USING SECTION

■ 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

OTC - STOP USE SECTION

■ 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

Ask Doctor

OTC - ASK DOCTOR SECTION

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

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

store at room temperature, not to exceed 86°F (30°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Artemisia vulgaris top oil, Cinnamon, Wormwood, Osmanthus fragrans flower, Eucalyptus oil, Saffron, Ginger,Adhesive

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2700159camphor 1.5 % / menthol 1 % Medicated PatchPSN2
2700159camphor 0.015 MG/MG / menthol 0.01 MG/MG Medicated PatchSCD2
2700159camphor 1.5 % / menthol 1 % Medicated PatchSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136950562995129GTIN-13: 6950562995129
EAN-13: 6950562995129
GTIN storage (14 digits): 06950562995129
Label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69561-006-01Herbal Knee Patch24 in 1 BOXPATCH242

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69561-00669561-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Herbal Knee PatchHERBAL KNEE PATCHHenan Kangdi Medical Devices Co., Ltd2a009059-b515-8214-e063-6294a90a4ed32026-02-07WarningsExact identifier
ndc (package): 69561-006-01
ndc (product): 69561-006
ndc11 (package): 69561000601
spl id: 4a3834f3-bae4-1aab-e063-6394a90ae152
spl set id: 2a009059-b515-8214-e063-6294a90a4ed3

Reported adverse events (FAERS/openFDA)#

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