TINNITUS RELINF PATCHES- camphor, borneol patch

TINNITUS RELINF PATCHES by

Drug Labeling and Warnings

TINNITUS RELINF PATCHES by is a Otc medication manufactured, distributed, or labeled by Shenzhen Furuizhilian keji Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Camphor 3%

Borneol 4%

PURPOSE

Topical analgesic

INDICATIONS & USAGE

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

WARNINGS

For external use only

DO NOT USE

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

WHEN USING

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

STOP USE

■ 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

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TINNITUS RELINF PATCHES 
camphor, borneol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84445-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BORNEOL (UNII: M89NIB437X) (BORNEOL - UNII:M89NIB437X)	BORNEOL	2.4 g  in 60 g
CAMPHOR, (-)- (UNII: 213N3S8275) (CAMPHOR, (-)- - UNII:213N3S8275)	CAMPHOR, (-)-	1.8 g  in 60 g

Inactive Ingredients
Ingredient Name	Strength
FU LING (UNII: XH37TWY5O4)
TANGERINE PEEL (UNII: JU3D414057)
MAGNOLIA OBOVATA BARK (UNII: SM9Z2LD5TK)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
ATRACTYLODES MACROCEPHALA ROOT (UNII: 08T3N29QJB)
ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84445-007-01	60 g in 1 BOX; Type 0: Not a Combination Product	07/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/17/2024

Labeler - Shenzhen Furuizhilian keji Co., Ltd. (418598613)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Furuizhilian keji Co., Ltd.		418598613	manufacture(84445-007)