FDA.reportPublic FDA data

Pain Relief Patch

Manufacturer
Anhui Miao De Tang Pharmaceutical Co., Ltd.
Effective date
2023-11-14
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:02:04

Label at a glance#

ProductPain Relief Patch
Active ingredientCAMPHOR (SYNTHETIC), METHYL SALICYLATE, MENTHOL
Label structure13 sections

Dosage and administration

For temporary relief of minor aches and pains. ​

Storage and handling

Store in clean, dry place outside of direct sunlight. Protect from excessive moisture.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Pain Relief Patchs

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.8g/patch
Menthol 5.2g/patch
Methyl Salicylate 3.1g/patch

Purpose

OTC - PURPOSE SECTION

Topical Analgesic, Pain Relief Patch

Use

INDICATIONS & USAGE SECTION

Use to the adjuvant treatment of pain caused by cervical spondylosis, frozen shoulder, lumbar disc herniation, rheumatoid arthritis, and bone or joint or soft tissue injury.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • On wounds or damaged skin
  • With a heating pad
  • If you are allergic to any ingredients of this product

OTC - WHEN USING SECTION

  • Use only as directed
  • Avoid contact with eyes, mucous membranes or rashes
  • Do not bandage tightly
  • Do not use at the same time as other topical analgesics
  • Dispose of used patch in manner that keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

OTC - STOP USE SECTION

  • If rash, itching or excessive skin irritation develops
  • If condition worsens
  • if symptoms last more than 7 days or clear up and occur again with 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For temporary relief of minor aches and pains.


​

Other information

STORAGE AND HANDLING SECTION

  • Store in clean, dry place outside of direct sunlight. Protect from excessive moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Colophony
Lanolin
Borneol
Vaseline
Natural Rubber

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81484-201-022024-07-30C16284748780-11e7a6dab-1b98-a2ce-e063-dadaa90aadf7Pain Relief Patch
81484-201-032024-07-30C16284748780-11e7a6dab-1b98-a2ce-e063-dadaa90aadf7Pain Relief Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81484-201-01Pain Relief Patch5 in 1 BAGPATCH55
81484-201-02Pain Relief Patch2 in 1 BOXPATCH25
81484-201-03Pain Relief Patch10 in 1 BOXPATCH105

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81484-201PAIN RELIEF PATCH (CAMPHOR, MENTHOL, METHYL SALICYLATE) PATCH [ANHUI MIAO DE TANG PHARMACEUTICAL CO., LTD.]5Legacy NDC, 3 package rows20231115_bf5f4da4-a8ab-ccc7-e053-2a95a90a0b9a.zip

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
81484-20181484-201-01, 81484-201-02, 81484-201-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
NATURAL LATEX RUBBER2LQ0UUW8INIACT
LANOLIN7EV65EAW6HIACT
BORNEOLM89NIB437XIACT
PETROLATUM4T6H12BN9UIACT
METHYL SALICYLATELAV5U5022YACTIB
ROSIN88S87KL877IACT
MENTHOLL7T10EIP3AACTIB

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
0a28578b-717a-7e42-e063-6294a90aaec6bf5f4da4-a8ab-ccc7-e053-2a95a90a0b9a2023-11-14WarningsExact identifier
spl id: 0a28578b-717a-7e42-e063-6294a90aaec6
spl set id: bf5f4da4-a8ab-ccc7-e053-2a95a90a0b9a

Reported adverse events (FAERS/openFDA)#

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