FDA.reportPublic FDA data

Pain Relief Patch

Manufacturer
Dengzhou Juhetang Medical Equipment Co., Ltd
Effective date
2024-03-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:09:30

Label at a glance#

ProductPain Relief Patch
Active ingredientWORMWOOD
Label structure13 sections

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

PAIN RELIEF PATCH

OTC - ACTIVE INGREDIENT SECTION

Wormwood 24%

OTC - PURPOSE SECTION

Topical analgesic

INDICATIONS & USAGE SECTION

For temporary relief of pain

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

more than 1 patch at a time
with a heating pad
on wounds or damaged skin
if you are allergic to any ingredients of this product

OTC - WHEN USING SECTION

use only as directed
do not bandage tightly
avoid contact with the eyes, mucous membranes or rashes

OTC - STOP USE SECTION

symptoms persist for more than 7 days
conditions worsen
symptoms clear up and occur again within a few days
Localized,skin,reactions,such as rash,itching,redness ,pain,swelling and blistering develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.lf 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 affected area
apply 1 patch at a time to affected area,not more than 3 to 4 times daily
remove film from patch and apply to the skin
Children under 12 years of age:consult a doctor

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

Safflower
Panax Notoginseng Root
Lycopodium Japonicum Whole
Ligusticum Sinense Subsp.Chuanxiong Whole
Parsnip
Gentiana Macrophylla Whole
Stephania Retrandra Root
Salvia Miltiorrhiza Whole

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label-1label-1label2label2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84171-101-012025-07-29C16284748780-13b156c62-2dfb-fb37-e063-e6dba90a4e07PAIN RELIEF PATCH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84171-101-01Pain Relief Patch12 in 1 PATCHPATCH123

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84171-101PAIN RELIEF PATCH (WORMWOOD) PATCH [DENGZHOU JUHETANG MEDICAL EQUIPMENT CO., LTD]31 package rows20240308_130f5915-7a61-ff5e-e063-6294a90a3031.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
84171-10184171-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
LYCOPODIUM JAPONICUM WHOLEOEI21JSS1RIACT
PANAX NOTOGINSENG ROOTGQX1C1175UIACT
GENTIANA MACROPHYLLA WHOLE5HGH7AO55YIACT
STEPHANIA TETRANDRA ROOT48PS81XHK0IACT
SALVIA MILTIORRHIZA WHOLE714783Y9Z0IACT
PARSNIPL2V28YP49SIACT
WORMWOODF84709P2XVACTIB
SAFFLOWER4VBL71TY4YIACT
LIGUSTICUM SINENSE SUBSP. CHUANXIONG WHOLECAX256379FIACT

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
13110257-e0ca-6292-e063-6294a90ab423130f5915-7a61-ff5e-e063-6294a90a30312024-03-07WarningsExact identifier
spl id: 13110257-e0ca-6292-e063-6294a90ab423
spl set id: 130f5915-7a61-ff5e-e063-6294a90a3031

Reported adverse events (FAERS/openFDA)#

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