ZHUANG GU SHE XIANG ZHI TONG GAO- camphor, menthol plaster

Zhuang Gu She Xiang Zhi Tong Gao by

Drug Labeling and Warnings

Zhuang Gu She Xiang Zhi Tong Gao by is a Otc medication manufactured, distributed, or labeled by Henan Lingrui Pharmaceutical Co.; Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Camphor  3.0%

Menthol 2.9%

PURPOSE

Camphor   External Analgesic

Menthol    External Analgesic

USES

For the temporary relief of minor aches and pains of muscles and joints due to:

simple backache

arthritis

strains

bruises

sprains

Warning

For External use only.

Allergy alert: This product contains natural rubber latex which may cause allergic reactions.

Do not use

on wounds

on irritated or damaged skin

if the appearance of this product has changed

in excess of 12 hours

if you have known hypersensitives to this product

otherwise than as directed

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

pregnant

taking other medications

WHEN USING THIS PRODUCT

avoid contact with the eye or mucous membrances

do not bandage tightly

supervise use by children

use caution if prone to allergic reactions

STOP USE AND ASK A DOCTOR IF

condition worsens

symptoms persist for more than 7 days

symptoms clear up and occur again within a few days

excessive irritaion of the skin develops

when using for pain of athritis

pain persists for more than 10 days

redness is present

in conditions affecting children under 12 years of age

Keep out of reach of children.

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

DIRECTIONS

Adults and children 12 years of age and older: Apply one or two plasters to affected area once a day. Remove after 12 hours.
Children 2 to 12 years of age and adults with compromised health: Use only under the guidance of a doctor.
Children under 2 years of age: Do not use, consult a doctor.
Refer to the above warnings: use otherwise than as directed may be dangerous.

Other Information

Keep container tightly closed.

Store below 20 degree centigrade (68 E F) in a dry area.

Inactive Ingredients

BOSWELLIA SACRA BARK, COMMIPHORA MYRRHA TOP, CLOVE, CINNAMOMUM AROMATICUM WHOLE, SCHIZONEPETA TENUIFOLIA WHOLE, SAPOSHNIKOVIA DIVARICATA ROOT, GERANIUM WILFORDII TOP, PERIPLOCA SEPIUM ROOT BARK, DRYNARIA FORTUNEI ROOT, ANGELICA DAHURICA ROOT, GINGER, BORNEOL, BELLADONNA LEAF, NATURAL LATEX RUBBER, ROSIN, ZINC OXIDE, LANOLIN, PARAFFIN, DIMETHYL SULFOXIDE, ANTIOXIDANT 119, METHYL SALICYLATE, MUSK KETONE

Questions or Comments?

E-mail: info@bjwellspring.com

Drug Facts

INGREDIENTS AND APPEARANCE

ZHUANG GU SHE XIANG ZHI TONG GAO 
camphor, menthol plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42217-203
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	3.0 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2.9 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BOSWELLIA SACRA BARK (UNII: 1UK28DX728)
COMMIPHORA MYRRHA TOP (UNII: N534J96ODY)
CLOVE (UNII: K48IKT5321)
CINNAMOMUM AROMATICUM WHOLE (UNII: 9BPF21T8ZR)
SCHIZONEPETA TENUIFOLIA WHOLE (UNII: C1107616TR)
SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
GERANIUM WILFORDII TOP (UNII: 771B1S9W3R)
PERIPLOCA SEPIUM ROOT BARK (UNII: 638OW484M3)
DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
GINGER (UNII: C5529G5JPQ)
BORNEOL (UNII: M89NIB437X)
BELLADONNA LEAF (UNII: 6GZW20TIOI)
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
ROSIN (UNII: 88S87KL877)
ZINC OXIDE (UNII: SOI2LOH54Z)
LANOLIN (UNII: 7EV65EAW6H)
PARAFFIN (UNII: I9O0E3H2ZE)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
ANTIOXIDANT 119 (UNII: UBL01213LI)
METHYL SALICYLATE (UNII: LAV5U5022Y)
MUSK KETONE (UNII: 483V3E1L6J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42217-203-10	10 in 1 BOX
1		1 g in 1 PATCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/02/2010

Labeler - Henan Lingrui Pharmaceutical Co.; Ltd (530021062)

Registrant - Henan Lingrui Pharmaceutical Co.; Ltd (530021062)

Establishment
Name	Address	ID/FEI	Business Operations
Henan Lingrui Pharmaceutical Co.; Ltd		530021062	manufacture(42217-203)