FDA.reportPublic FDA data

Sun Moon Star

Manufacturer
Kingsway Trading | Licoman Herbal Research Lab Limited
Effective date
2011-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:29:01

Label at a glance#

ProductSun Moon Star Pain Relieving
Active ingredientMenthol, Methyl Salicylate
Label structure10 sections

Indications and uses

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 16%
Methyl Salicylate 15%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor pains and aches of muscles and joints  associated with:

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

  • For external use only
  • avoid getting into the eyes or on mucus membranes.
 

When using this product

OTC - WHEN USING SECTION

  • do not apply to wound or damaged skin.
  • do not bandage tightly
  • do not use otherwise than as directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
  • pain persists for more than 10 days
  • redness is present
  • conditions affect children under 12 years of age

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning. In case of accidental ingestion, contact a doctor or Poison Control Center immediately

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 12 years of age and older:
  • if necessary cut patch to size
  • remove protective backing and apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age:do not use, consult a doctor

INACTIVE INGREDIENT SECTION

Inactive Ingredients Angelica root, Cang-zhu atractylodes rhizome, Chinese peony root, Dong Quai root, Fo-ti root,  Large leaf gentian root, Oleo gum resin, Notopterygium root, Phellodendron bark, Schizonepeta, and Skullcap root

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label
image of package label
image of package label


FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63922-222-012019-10-29C16284748780-1960f7f55-cb1e-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63922-222-01Sun Moon Star Pain Relieving5 in 1 BOXPATCH51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63922-222SUN MOON STAR (MENTHOL METHYL SALICYLATE) PATCH [KINGSWAY TRADING]1Legacy NDC, 1 package rows20110801_763c20db-ab44-4683-ab6f-e2bde735880a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MentholACTIVE INGREDIENTL7T10EIP3A1
Methyl SalicylateACTIVE INGREDIENTLAV5U5022Y1
MentholACTIVE MOIETYL7T10EIP3A1
Methyl SalicylateACTIVE MOIETYLAV5U5022Y1
ANGELICA ARCHANGELICA ROOTINACTIVE INGREDIENTDTN01M69SN1
ANGELICA SINENSIS ROOTINACTIVE INGREDIENTB66F4574UG1
ATRACTYLODES LANCEA ROOTINACTIVE INGREDIENTCAZ6282J2O1
GENTIANA MACROPHYLLA ROOTINACTIVE INGREDIENT6559FC0U1B1
NOTOPTERYGIUM FRANCHETII ROOTINACTIVE INGREDIENTKRT28P6ITK1
PHELLODENDRON CHINENSIS BARKINACTIVE INGREDIENT2866QMZ4341

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63922-22263922-222-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
MentholL7T10EIP3AACTIB
Methyl SalicylateLAV5U5022YACTIB
ANGELICA ARCHANGELICA ROOTDTN01M69SNIACT
ATRACTYLODES LANCEA ROOTCAZ6282J2OIACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
GENTIANA MACROPHYLLA ROOT6559FC0U1BIACT
NOTOPTERYGIUM FRANCHETII ROOTKRT28P6ITKIACT
PHELLODENDRON CHINENSIS BARK2866QMZ434IACT

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
2be7ff9e-918c-4424-95e9-8f74f79b1f37763c20db-ab44-4683-ab6f-e2bde735880a2011-07-13WarningsExact identifier
spl id: 2be7ff9e-918c-4424-95e9-8f74f79b1f37
spl set id: 763c20db-ab44-4683-ab6f-e2bde735880a

Reported adverse events (FAERS/openFDA)#

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