She Xiang Zhuang Gu Gao

Manufacturer
Inner Mongolia Horqin Pharmaceutical Co., Ltd
Effective date
2019-03-14
Label type
HUMAN OTC DRUG LABEL
Version
32505
Source
full-release
Hydrated at
2026-05-31 22:58:58

Label at a glance#

ProductShe Xiang Zhuang Gu Gao
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure15 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints due to: simple backache arthritis strains bruises sprains

Dosage and administration

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.

Storage and handling

Keep container tightly closed. Store below 20ºC  (68°F) in a dry area.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Camphor    1.91%

Menthol      2.54%

Methyl Salicylete     1.62%

PURPOSE

OTC - PURPOSE SECTION

Camphor   External Analgesic

Menthol     External Analgesic

Methyl Salicylate   External Analgesic

USES

INDICATIONS & USAGE SECTION

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

simple backache

arthritis

strains

bruises

sprains

Warnings

WARNINGS SECTION

For External Use only.

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

Do not use

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR/PHARMACIST SECTION

pregnant

taking other medications

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

Keep container tightly closed.

Store below 20ºC  (68°F) in a dry area.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

E-mail: info@magicwandbj.com

Exclusive Overseas Sales

SPL UNCLASSIFIED SECTION

Magic Wand (Beijing) Trading Company Limited

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2120570camphor 1.91 % / menthol 2.54 % / methyl salicylate 1.62 % Medicated PatchPSN32505
2120570camphor 0.0191 MG/MG / menthol 0.0254 MG/MG / methyl salicylate 0.0162 MG/MG Medicated PatchSCD32505
2120570camphor 1.91 % / menthol 2.54 % / methyl salicylate 1.62 % Medicated PatchSY32505

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72963-001-022021-01-29C16284748780-1ba0f9c33-43d7-a910-e053-dadaa90a0b85Inner Mongolia Horqin Pharmaceutical Co., Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72963-001-02She Xiang Zhuang Gu Gao10 in 1 BOXPLASTER1032505
72963-001-02She Xiang Zhuang Gu Gao2.98 g in 1 PATCHPLASTER2.9832505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72963-001SHE XIANG ZHUANG GU GAO (CAMPHOR, MENTHOL, METHYL SALICYLATE) PLASTER [INNER MONGOLIA HORQIN PHARMACEUTICAL CO., LTD]32505Legacy NDC, 2 package rows20190326_84af7160-b3be-40fa-abb5-65dd335d4b69.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72963-00172963-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
614d4a23-b450-431a-8fc5-ceda6ffe2a5684af7160-b3be-40fa-abb5-65dd335d4b692019-03-14WarningsExact identifier
spl id: 614d4a23-b450-431a-8fc5-ceda6ffe2a56
spl set id: 84af7160-b3be-40fa-abb5-65dd335d4b69

Reported adverse events (FAERS/openFDA)#

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