Knee Pain Relief Patch

Manufacturer
Anhui Miao De Tang Pharmaceutical Co., Ltd.
Effective date
2023-11-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:02:05

Label at a glance#

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

Storage and handling

Avoid storing the product in direct sunlight. Protect from excessive moisture.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Knee Pain Relief Patch

OTC - ACTIVE INGREDIENT SECTION

DL-Camphor 1.2% / Topical Analgesic

L-Menthol 5.7% / Topical Analgesic

Methyl Salicylate6.3% / Topical Analgesic

OTC - PURPOSE SECTION

Topical Analgesic,Knee Pain Relief Patch

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints associated with:Arthritis,Strains,Bruises,Sprains

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on wounds or damaged skin
If you are allergic to aspirin or salicylates.
With a heating pad.
With, or at the same time as, other external analgesic products.

OTC - WHEN USING SECTION

When using this product:

Use only as directed.
Avoid contact with the eyes, mucous membranes, or rashes.

OTC - STOP USE SECTION

Rash, itching, or excessive skin irritation develops.

Conditions worsen.
Symptoms persist for more than 7 days.
Symptoms clear up then occur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over:
Clean and dry the affected area.
Remove a patch from the film.
Apply the patch to the affected area for not more than 3 to 4 times a day for 7 days.`
You can wear the patch for up to 8 hours per application.
Consult a doctor

STORAGE AND HANDLING SECTION

Avoid storing the product in direct sunlight. Protect from excessive moisture.

INACTIVE INGREDIENT SECTION

Dried Ginger, Cinnamon, Orange Peel, Glycerol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Knee Pain Relief PatchKnee Pain Relief Patch

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2717562camphor 1.2 % / levomenthol 5.7 % / methyl salicylate 6.3 % Medicated PatchPSN4
2717562camphor 0.012 MG/MG / levomenthol 0.057 MG/MG / methyl salicylate 0.063 MG/MG Medicated PatchSCD4
2717562camphor 1.2 % / levomenthol 5.7 % / methyl salicylate 6.3 % Medicated PatchSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81484-401-022024-07-30C16284748780-11e7a6dab-18bf-a2ce-e063-dadaa90aadf7Knee Pain Relief Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81484-401-01Knee Pain Relief Patch2 in 1 BAGPATCH24
81484-401-02Knee Pain Relief Patch7 in 1 BOXPATCH74

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81484-401KNEE PAIN RELIEF PATCH (CAMPHOR, MENTHOL, METHYL SALICYLATE) PATCH [ANHUI MIAO DE TANG PHARMACEUTICAL CO., LTD.]4Legacy NDC, 2 package rows20231115_dfb9861a-74eb-5c7c-e053-2a95a90ac7bd.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81484-40181484-401-01, 81484-401-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
0a283b77-4b25-370d-e063-6294a90ae4dfdfb9861a-74eb-5c7c-e053-2a95a90ac7bd2023-11-14WarningsExact identifier
spl id: 0a283b77-4b25-370d-e063-6294a90ae4df
spl set id: dfb9861a-74eb-5c7c-e053-2a95a90ac7bd

Reported adverse events (FAERS/openFDA)#

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