FDA.reportPublic FDA data

Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster

Manufacturer
International Nature Nutraceuticals | Henan Lingrui Pharmaceutical Co., Ltd
Effective date
2013-12-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:37:55

Label at a glance#

ProductZhuanggu Shexiang Zhitonggao Pain Relieving Plaster
Active ingredientCAMPHOR (NATURAL), MENTHOL, METHYL SALICYLATE
Label structure11 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 the guidance of a doctor Children under 2 years of age: do not use

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor-3.0%
Menthol- 2.9%

Methyl Salicylate- 10.4%

Uses

OTC - PURPOSE 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

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 known sensitivity this product

Ask a doctor or pharmacist before use if you are:

OTC - ASK DOCTOR/PHARMACIST SECTION

Pregnant, or taking other medications

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children

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 the guidance of a doctor

Children under 2 years of age: do not use

Storage

INDICATIONS & USAGE SECTION

Store at 15o C to 30o C (59o to 86o F)

Keep away from heat

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Frankincense, Myrrh, Schizonepeta tenuifolia flowering top, Saposhnikovia divaricata root, Chinese Cinnamon, Atropa belladona, natural latex rubber, rosin, aconitum kusnezoffi root, aconitum carmichaelii root, strychons nux-vomica seed, clove, erodium stephanianum top, periploca sepium root bark

package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51367-019-102019-11-27C16284748780-19855e2a2-3dad-60a7-e053-dbdaa90a05bdDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51367-019-10Zhuanggu Shexiang Zhitonggao Pain Relieving Plaster10 in 1 BOXPLASTER101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51367-019ZHUANGGU SHEXIANG ZHITONGGAO PAIN RELIEVING PLASTER (CAMPHOR, MENTHOL, METHYL SALICYLATE) PLASTER [INTERNATIONAL NATURE NUTRACEUTICALS]1Legacy NDC, 1 package rows20131228_df0e307f-8612-4bb2-bee3-a91f1b2ab1ba.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9411
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y1
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9411
MENTHOLACTIVE MOIETYL7T10EIP3A1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
ACONITUM CARMICHAELII ROOTINACTIVE INGREDIENTXJ28061U1S1
ACONITUM KUSNEZOFFII ROOTINACTIVE INGREDIENT3L29I4K8KX1
ATROPA BELLADONNAINACTIVE INGREDIENTWQZ3G9PF0H1
CHINESE CINNAMONINACTIVE INGREDIENTWS4CQ062KM1
CLOVEINACTIVE INGREDIENTK48IKT53211
ERODIUM STEPHANIANUM TOPINACTIVE INGREDIENT5307U0XCAS1
FRANKINCENSEINACTIVE INGREDIENTR9XLF1R1WM1
MYRRHINACTIVE INGREDIENTJC71GJ1F3L1
NATURAL LATEX RUBBERINACTIVE INGREDIENT2LQ0UUW8IN1
PERIPLOCA SEPIUM ROOT BARKINACTIVE INGREDIENT638OW484M31
ROSININACTIVE INGREDIENT88S87KL8771
SAPOSHNIKOVIA DIVARICATA ROOTINACTIVE INGREDIENT8H84LFK2QD1
SCHIZONEPETA TENUIFOLIA FLOWERING TOPINACTIVE INGREDIENT2FN3BA1MZE1
STRYCHNOS NUX-VOMICA SEEDINACTIVE INGREDIENT269XH139191

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51367-01951367-019-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (NATURAL)N20HL7Q941ACTIB
MENTHOLL7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
FRANKINCENSER9XLF1R1WMIACT
MYRRHJC71GJ1F3LIACT
SCHIZONEPETA TENUIFOLIA FLOWERING TOP2FN3BA1MZEIACT
CHINESE CINNAMONWS4CQ062KMIACT
SAPOSHNIKOVIA DIVARICATA ROOT8H84LFK2QDIACT
ATROPA BELLADONNAWQZ3G9PF0HIACT
NATURAL LATEX RUBBER2LQ0UUW8INIACT
ROSIN88S87KL877IACT
ACONITUM KUSNEZOFFII ROOT3L29I4K8KXIACT
ACONITUM CARMICHAELII ROOTXJ28061U1SIACT
STRYCHNOS NUX-VOMICA SEED269XH13919IACT
CLOVEK48IKT5321IACT
ERODIUM STEPHANIANUM TOP5307U0XCASIACT
PERIPLOCA SEPIUM ROOT BARK638OW484M3IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ROSINROSIN88S87KL877TABLET, COATED / ORAL10 mgExact identifier — unii candidate
3 equally ranked IID candidates
ROSINROSIN88S87KL877TABLET, EXTENDED RELEASE / ORAL8.99 mgExact identifier — unii candidate
3 equally ranked IID candidates
ROSINROSIN88S87KL877CAPSULE / ORALNAExact identifier — unii candidate
3 equally ranked IID candidates

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
65c1715d-d205-4b3e-81f8-9d40db26cb72df0e307f-8612-4bb2-bee3-a91f1b2ab1ba2013-12-27WarningsExact identifier
spl id: 65c1715d-d205-4b3e-81f8-9d40db26cb72
spl set id: df0e307f-8612-4bb2-bee3-a91f1b2ab1ba

Reported adverse events (FAERS/openFDA)#

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