Knee Pain Relief Patch

Manufacturer
Anhui Miao De Tang Pharmaceutical Co., Ltd.
Effective date
2024-01-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:06:57

Label at a glance#

ProductKnee Pain Relief Patch
Active ingredientMETHYL SALICYLATE, CAMPHOR (SYNTHETIC), MENTHOL
Label structure13 sections

Storage and handling

avoid storing in direct sunlight protect from excessive moisture

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Knee Pain Relief Patch

OTC - ACTIVE INGREDIENT SECTION

camphor 3.1%
menthol 6%
methyl salicylate 10%

OTC - PURPOSE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with.
simple backache.
arthritis.
strains.
bruises.
sprains.

INDICATIONS & USAGE SECTION

Adults and children 2 years of age and older
clean and dry the affected area.
remove the patch from the release liner.
apply to affected area not more than 3 to 4 times daily.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Children under 2 years of age
do not use, consult a doctor

OTC - WHEN USING SECTION

use only as directed.
avoid contact with the eyes.
do not apply to wounds or damaged skin.
do not bandage tightly.

OTC - STOP USE SECTION

if condition worsens.
if symptoms persist for more than 7 days.
if symptoms clear up and occur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

apply to affected area not more than 3 to 4 times daily

STORAGE AND HANDLING SECTION

avoid storing in direct sunlight

protect from excessive moisture

INACTIVE INGREDIENT SECTION

eucalyptus, peppermint, thyme, wintergreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1793147camphor 3.1 % / menthol 6 % / methyl salicylate 10 % Medicated PatchPSN1
1793147camphor 0.031 MG/MG / menthol 0.06 MG/MG / methyl salicylate 0.1 MG/MG Medicated PatchSCD1
1793147camphor 3.1 % / menthol 6 % / methyl salicylate 10 % Medicated PatchSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81484-102-022024-07-30C16284748780-11e7a6dab-16b0-a2ce-e063-dadaa90aadf7Knee Pain Relief Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81484-102-01Knee Pain Relief Patch2 in 1 BAGPATCH21
81484-102-02Knee Pain Relief Patch7 in 1 BOXPATCH71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81484-102KNEE PAIN RELIEF PATCH (CAMPHOR, MENTHOL, METHYL SALICYLATE) PATCH [ANHUI MIAO DE TANG PHARMACEUTICAL CO., LTD.]12 package rows20240111_0e7ffc0f-e2b9-377c-e063-6294a90a29d6.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81484-10281484-102-01, 81484-102-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
0e7ffc0f-e2ba-377c-e063-6294a90a29d60e7ffc0f-e2b9-377c-e063-6294a90a29d62024-01-09WarningsExact identifier
spl id: 0e7ffc0f-e2ba-377c-e063-6294a90a29d6
spl set id: 0e7ffc0f-e2b9-377c-e063-6294a90a29d6

Reported adverse events (FAERS/openFDA)#

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