Label: SHANG SHI ZHI TONG GAO- camphor, menthol, methyl salicylate plaster

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 27, 2014

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENTS

    Camphor 3.0%

    Menthol 1.5%

    Methyl Salicylate 2.5%

  • PURPOSE

    Camphor   External Analgesic

    Menthol     External Analgesic

    Methyl Salicylate   External Analgesic

  • USES

    To relieve the rheumatic pain and arthralgia by promoting blood circulation, used for rheumatoid arthristis muscular aches, sprain etc.

  • WARNINGS

    For external use only.

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

  • DO NOT USE

    Do not use

    on wounds.

    on irritated or damaged skin

    if the apperance of this product has changed

    in excess of 12 hours

    if you have know hypersensitivities to this product

    otherwise than as directed

  • Ask a Doctor or Pharmacist before use if you are

    Pregnent

    taking other medications

  • When using this product

    avoid contact iwth the eyes 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

    symptonms persist for more than 7 days

    symptoms clear up and occur again within 1 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

  • Keep out of reach of children.

    Keep out of reach of children. If swallowed, get medical help or Poison Control Center right away.

  • Adults and children 12 years of age and older: Apply one or two plasters to affected area once a day. Remove after 12 hours.DIRECTIONBRefer to the above warnings: use otherwise than as directed may be dangerous.

    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

  • Questions or Commnets?

    E-mail: info@bjwellspring.com

  • DRUG FACTS

    image description

  • INGREDIENTS AND APPEARANCE
    SHANG SHI ZHI TONG GAO 
    camphor, menthol, methyl salicylate plaster
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42217-201
    Route of AdministrationTRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)3.0 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.5 g  in 100 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE2.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42217-201-1010 in 1 BOX
    11 g in 1 PATCH
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34806/02/2010
    Labeler - Henan Lingrui Pharmaceutical Co.; Ltd (530021062)
    Registrant - Henan Lingrui Pharmaceutical Co.; Ltd (530021062)
    Establishment
    NameAddressID/FEIBusiness Operations
    Henan Lingrui Pharmaceutical Co.; Ltd530021062manufacture(42217-201)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!