Label: LA VAQUITA NEW EXTRA- methyl salicylate, menthol ointment

  • NDC Code(s): 61734-301-01, 61734-301-02
  • Packager: Delon Laboratories (1990) Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 24, 2023

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  • Active ingredients

    Menthol 3%

    Methyl Salicylate 12%

  • Purpose

    Topical analgesic

  • Uses

    • for the temporary relief of minor aches and pains of muscles and joints

  • Warnings

    For external use only

    When using this product

    • avoid contact with the eyes
    • do not bandage tightly
    • do not apply to wounds or damaged skin

    Stop use and ask a doctor if

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


    If pregnant or breast-feeding, ask a health professional before use.

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

  • Directions

    • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: consult a doctor

  • Inactive ingredients


    D&C red no. 17, lanolin, paraffin, petrolatum

  • PRINCIPAL DISPLAY PANEL

    La Vaquita Extra 90g

  • PRINCIPAL DISPLAY PANEL

    La Vaquita Extra 100g

  • INGREDIENTS AND APPEARANCE
    LA VAQUITA  NEW EXTRA
    methyl salicylate, menthol ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61734-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE12 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    LANOLIN (UNII: 7EV65EAW6H)  
    D&C RED NO. 17 (UNII: ND733RX3JN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61734-301-0190 g in 1 CAN; Type 0: Not a Combination Product10/04/2014
    2NDC:61734-301-02100 g in 1 JAR; Type 0: Not a Combination Product07/18/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/26/2011
    Labeler - Delon Laboratories (1990) Ltd (248364184)
    Establishment
    NameAddressID/FEIBusiness Operations
    Laboratoires Delon208896216label(61734-301) , manufacture(61734-301) , pack(61734-301)
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