Label: SINSIN MULPAS- camphor, menthol, methyl salicylate liquid

  • NDC Code(s): 55264-007-01, 55264-007-02
  • Packager: Sinsin Pharmaceutical Co., Ltd.
  • 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 24, 2023

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  • Active ingredients

    DL-Camphor 4.5%

    L-Menthol 4.2%

    Methyl Salicylate 6.9%

  • Purpose

    Topical Analgesic

  • Uses

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

    • arthritis
    • simple backache
    • strains
    • bruises
    • sprains
  • Warnings

  • For external use only.

    Flammable

    keep away from fire, sparks and heated surfaces

  • Do not use

    • on wounds or damaged skin
  • When using this product

    • do not bandage tightly
    • avoid contact with the eyes mucous membranes
  • Stop use and ask a doctor if

    condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days

  • 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 over:

    • adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily.
    • children under 2 years of age: consult a doctor

    Children under 12 years of age:

    • Consult a doctor.
  • Inactive ingredients

    Concentrated Glycerin, Chlorpheniramine Maleate, Ethanol (synthetic), Purified Water, Thymol

  • Manufactured by:

    SINSIN PHARM. CO., LTD.

    90, Beomjigi-ro 141 beon-gil, Danwon-Gu, Ansan-si, Gyeonggi-do, Korea

    http://www.sinsin.com    tel: 82-31-776-1140~3

  • Principal Display Panel

    Mulpas Display
  • INGREDIENTS AND APPEARANCE
    SINSIN MULPAS 
    camphor, menthol, methyl salicylate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55264-007
    Route of AdministrationTOPICAL, CUTANEOUS, TRANSDERMAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)4.5 mg  in 1 mL
    LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL4.2 mg  in 1 mL
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE6.9 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    THYMOL (UNII: 3J50XA376E)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55264-007-021 in 1 CARTON11/09/2018
    1NDC:55264-007-01120 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34801/10/2014
    Labeler - Sinsin Pharmaceutical Co., Ltd. (823149161)
    Registrant - Sinsin Pharmaceutical Co., Ltd. (823149161)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sinsin Pharmaceutical Co., Ltd.687867143manufacture(55264-007)
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