SHE XIANG ZHUANG GU GAO- camphor, menthol, methyl salicylate plaster

She Xiang Zhuang Gu Gao by

Drug Labeling and Warnings

She Xiang Zhuang Gu Gao by is a Otc medication manufactured, distributed, or labeled by Inner Mongolia Horqin Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Camphor    1.91%

Menthol      2.54%

Methyl Salicylete     1.62%

PURPOSE

Camphor   External Analgesic

Menthol     External Analgesic

Methyl Salicylate   External Analgesic

USES

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

simple backache

arthritis

strains

bruises

sprains

Warnings

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 hypersensitive 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 membranes

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 irritation of the skin develops

when using for pain of arthritis

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 20ºC  (68°F) in a dry area.

Inactive Ingredients

STAR ANISE, ANGELICA DAHURICA ROOT, ATRACTYLODES LANCEA ROOT, ANGELICA SINENSIS ROOT, GINGER, CYNANCHUM PANICULATUM WHOLE, KAEMPFERIA GALANGA ROOT, GERANIUM WILFORDII WHOLE, CYATHULA OFFICINALIS ROOT, MUSCONE, CHONDROITIN SULFATE (PORCINE), BORNEOL, DIPHENHYDRAMINE HYGROCHLORIDE, NATURAL LATEX RUBBER, ROSIN, ZINC OXIDE, PETROLATUM, LANOLIN, PARAFFIN

Questions or Comments?

E-mail: info@magicwandbj.com

Exclusive Overseas Sales

Magic Wand (Beijing) Trading Company Limited

Drug Facts

INGREDIENTS AND APPEARANCE

SHE XIANG ZHUANG GU GAO 
camphor, menthol, methyl salicylate plaster

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72963-001
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	1.91 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2.54 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	1.62 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STAR ANISE (UNII: XKC1657P78)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
GINGER (UNII: C5529G5JPQ)
CYNANCHUM PANICULATUM WHOLE (UNII: T14ONG8D7H)
KAEMPFERIA GALANGA ROOT (UNII: 7B7U9D12AI)
GERANIUM WILFORDII WHOLE (UNII: QXI974Y72W)
CYATHULA OFFICINALIS ROOT (UNII: BRM37UP34O)
MUSCONE (UNII: UPS3C6CV36)
CHONDROITIN SULFATE (PORCINE) (UNII: V5E8ELO4W9)
BORNEOL (UNII: M89NIB437X)
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
ROSIN (UNII: 88S87KL877)
ZINC OXIDE (UNII: SOI2LOH54Z)
PETROLATUM (UNII: 4T6H12BN9U)
LANOLIN (UNII: 7EV65EAW6H)
PARAFFIN (UNII: I9O0E3H2ZE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72963-001-02	10 in 1 BOX	02/19/2019
1		2.98 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/19/2019

Labeler - Inner Mongolia Horqin Pharmaceutical Co., Ltd (548635483)

Registrant - Inner Mongolia Horqin Pharmaceutical Co., Ltd (548635483)

Establishment
Name	Address	ID/FEI	Business Operations
Inner Mongolia Horqin Pharmaceutical Co., Ltd		548635483	manufacture(72963-001)