FDA.reportPublic FDA data

Tinnitus patch

Manufacturer
Dengzhou Juhetang Medical Equipment Co., Ltd
Effective date
2024-03-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:09:30

Label at a glance#

ProductTinnitus patch
Active ingredientLONICERA CAPRIFOLIUM FLOWER
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

Tinnitus patch

OTC - ACTIVE INGREDIENT SECTION

Lonicera Caprifolium Flower 31%

OTC - PURPOSE SECTION

Topical analgesic

INDICATIONS & USAGE SECTION

Tinnitus Relief Promote blood circulation

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

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

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

forsythia suspensa root
Rhubarb
Xanthium
Angelica Dahurica Whole

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label3label3label4label4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84171-201-012025-07-29C16284748780-13b156c62-2af8-fb37-e063-e6dba90a4e07Tinnitus patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84171-201-01Tinnitus patch60 in 1 PATCHPATCH601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84171-201TINNITUS PATCH (LONICERA CAPRIFOLIUM FLOWER) PATCH [DENGZHOU JUHETANG MEDICAL EQUIPMENT CO., LTD]11 package rows20240308_13106229-138c-4a8a-e063-6394a90afcb9.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84171-20184171-201-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
LONICERA CAPRIFOLIUM FLOWER5N1WD9784UACTIB
XANTHIUM SIBIRICUM ROOT8555ORT735IACT
RHUBARBG280W4MW6EIACT
FORSYTHIA SUSPENSA ROOTYM9E56VP46IACT
ANGELICA DAHURICA WHOLE667W6C5J4PIACT

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
13106229-138d-4a8a-e063-6394a90afcb913106229-138c-4a8a-e063-6394a90afcb92024-03-07WarningsExact identifier
spl id: 13106229-138d-4a8a-e063-6394a90afcb9
spl set id: 13106229-138c-4a8a-e063-6394a90afcb9

Reported adverse events (FAERS/openFDA)#

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