TINNITUS RELINF PATCHES

Manufacturer
Shenzhen Furuizhilian keji Co., Ltd.
Effective date
2024-08-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:16:54

Label at a glance#

ProductTINNITUS RELINF PATCHES
Active ingredientCAMPHOR, (-)-, BORNEOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Camphor 3%

Borneol 4%

OTC - PURPOSE SECTION

Topical analgesic

INDICATIONS & USAGE SECTION

For temporary relief of minor aches & pains of muscles & joints associated with: arthritis, simple backache, strains, bruises, sprains

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

on 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 the eyes, mucous membranes or rashes.
do not bandage tightly

OTC - STOP USE SECTION

■ skin reactions such as redness, itching, rash, excessive irritation,burning sensation, swelling or blistering occur
■ symptoms persist for more than 7 days
■ symptoms clear up and occur again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 affected area
■ remove patch from film
■ apply to affected area not more than 3 to 4 times daily
■ remove patch from the skin after at most8-hour application
Children under 12 years of age:
consult a doctor

INACTIVE INGREDIENT SECTION

Artemisia Argyi Leaf Extract, Scutellaria Baicalensis Extract, Poria Cocos Extract, Atractylodes Macrocephala Root Extract, Tangerine Peel, Magnolia Bark Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84445-010-012025-07-29C16284748780-13b156c62-2963-fb37-e063-e6dba90a4e071f232a49-70aa-14f3-e063-6294a90a95a4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84445-010-01TINNITUS RELINF PATCHES28 in 1 BOXPATCH281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84445-010TINNITUS RELINF PATCHES (CAMPHOR, BORNEOL) PATCH [SHENZHEN FURUIZHILIAN KEJI CO., LTD.]11 package rows20240809_1f232a49-70aa-14f3-e063-6294a90a95a4.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
84445-01084445-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
1f232a49-70ab-14f3-e063-6294a90a95a41f232a49-70aa-14f3-e063-6294a90a95a42024-08-07WarningsExact identifier
spl id: 1f232a49-70ab-14f3-e063-6294a90a95a4
spl set id: 1f232a49-70aa-14f3-e063-6294a90a95a4

Reported adverse events (FAERS/openFDA)#

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