Label: LIBERDOL TOPICAL ANALGESIC (methyl salicylate, menthol, camphor- synthetic spray

  • NDC Code(s): 71262-008-55
  • Packager: ViaDerma Distribution, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 1, 2023

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  • Drug Facts

  • Active Ingredient

    Methyl Salicylate 300mg

    Menthol 100mg

    Camphor 40mg

    Purpose

    Analgesic

  • Uses

    Soothing on-the-go tempoary relief from minor aches and pains of sore muscles and joint associated with:

    • arthritis
    • backache
    • strains
    • sprains
  • Warnings

    For external use only. : Keep away form excessive heat or open flame Flammable

    Ask a doctor before use if you have:

    Sensitive skin, are pregnant or are bleeding

    When using this product:

    • Avoid contact with eyes or mucus membranes
    • Do not apply to open wounds or damaged skin
    • Do not use with other ointments, creams, sprays or liniments
    • Do not apply to irritated skin, or if excessive irritation develops
    • Do not bandage
    • Do not use with heating pad or device

    Stop use and ask a doctor if:

    Condition worsens or if symptoms persist more than 7 days, or clear up or reoccur

    Keep out of reach of children.

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

  • Directions

    • Apply to affected areas not more than 4 times daily Adults and children 2 years of age an older: 
    • Consult a physician Children under 2 years of age:
  • Other Information

    • Store in a cool dry place out of direct sunlight
  • Inactive Ingredients

    acetic acid, arnica montana flower extract, ascorbic acid, chlorhexidine gluconate, cholecalciferol, dimethyl sulfoxide, dipropylene glycol, glucono delta lactone, glycerin, histidine, hydroxethyl cellulose, magnesium stearate, sodium hydroxide, sorbic acid, stearic acid, water

  • Package Labeling:

    Outer PackageInner Package

  • INGREDIENTS AND APPEARANCE
    LIBERDOL TOPICAL ANALGESIC 
    methyl salicylate, menthol, camphor (synthetic) spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71262-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE300 mg  in 1 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL100 mg  in 1 mL
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACETIC ACID (UNII: Q40Q9N063P)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HISTIDINE (UNII: 4QD397987E)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SORBIC ACID (UNII: X045WJ989B)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71262-008-551 in 1 CARTON06/01/2021
    155 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/01/2021
    Labeler - ViaDerma Distribution, Inc (081113521)
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