TINNITUS RELINF PATCHES

Manufacturer: Linhe Biotechnology (Shenzhen) Co., Ltd
Effective date: 2024-08-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:16:38

Label at a glance#

ProductTINNITUS RELINF PATCHES

Active ingredientBORNEOL, CAMPHOR, (-)-

Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Camphor 0.01%

Borneol 0.01%

OTC - PURPOSE SECTION

Topical analgesic

INDICATIONS & USAGE SECTION

For temporary relief of minor aches & pains of muscles 8 joints associated with arthritis, simple backache, strains, bruises, sprains

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

1.on damaged skin. 2.with a heating pad. 3.if you are allergic to any ingredients of this product.

OTC - WHEN USING SECTION

1.use only as directed. 2.avoid contact with the eyes, mucous membranes or rashes. 3.do not bandage tightly.

OTC - STOP USE SECTION

1.skin reactions such as redness, itching, rash, excessive irritation,burning sensation,sweling or blistering occur, 2.symptoms persist for more than 7 days. 3.symptoms clear up and occur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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:

1.clean and dry affected area. 2.remove patch from film. 3.opply to affected area not morethan 3 to f times daily. 4.remove patch from the skin after at most 8-hour application.

Children under 12 years of age:

Cansult a doctor.

INACTIVE INGREDIENT SECTION

Fu Ling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
84575-002-01	2025-07-29	C162847	48780-1	3b156c62-32b0-fb37-e063-e6dba90a4e07	TINNITUS RELINF PATCHES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84575-002-01	TINNITUS RELINF PATCHES	9 g in 1 BOX	PATCH	9		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84575-002	TINNITUS RELINF PATCHES (CAMPHOR, BORNEOL) PATCH [LINHE BIOTECHNOLOGY (SHENZHEN) CO., LTD]	1	1 package rows	20240807_1e83eedf-af49-9091-e063-6394a90ade67.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

TINNITUS RELINF PATCHES
Camphor, Borneol
BORNEOL
CAMPHOR, (-)-
FU LING

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84575-002	84575-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BORNEOL	M89NIB437X	ACTIB
CAMPHOR, (-)-	213N3S8275	ACTIB
FU LING	XH37TWY5O4	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1e83eedf-af4a-9091-e063-6394a90ade67			1e83eedf-af49-9091-e063-6394a90ade67	2024-08-01	Warnings	Exact identifier spl id: 1e83eedf-af4a-9091-e063-6394a90ade67 spl set id: 1e83eedf-af49-9091-e063-6394a90ade67

Reported adverse events (FAERS/openFDA)#

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