Label: MENTHOLATUM ORIGINAL- camphor, menthol ointment

  • NDC Code(s): 10742-0002-1, 10742-0002-2, 10742-0002-3, 10742-0002-4
  • Packager: The Mentholatum Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2024

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  • Active ingredients

    Camphor 9%

    Menthol 1.3%

  • Purpose

    Camphor - Topical Analgesic

    Menthol - Topical Analgesic

  • Uses

    temporarily relieves minor aches and pains of muscles and joints

  • Warnings

    For external use only

    When using this product

    • do not get into eyes
    • do not apply to wounds or to damaged skin
    • do not bandage tightly
    • do not heat, microwave, or add to hot water as this may cause splattering and result in burns

    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

    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 and over: apply to affected area not more than 3 to 4 times daily
    • children under 2 years: ask a doctor
  • Inactive ingredients

    fragrance, petrolatum, titanium dioxide

  • Questions?

    1-877-636-2677 MON-FRI 9AM to 5PM (EST)

  • Package/Label Principal Display Panel

    Mentholatum Original Ointment
  • INGREDIENTS AND APPEARANCE
    MENTHOLATUM  ORIGINAL
    camphor, menthol ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)90 mg  in 1 g
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM13 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10742-0002-11 in 1 CARTON12/01/2014
    128 g in 1 JAR; Type 0: Not a Combination Product
    2NDC:10742-0002-21 in 1 CARTON12/01/2014
    285 g in 1 JAR; Type 0: Not a Combination Product
    3NDC:10742-0002-31 in 1 CARTON10/19/2020
    334 g in 1 JAR; Type 0: Not a Combination Product
    4NDC:10742-0002-41 in 1 CARTON10/19/2020
    4102.1 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/01/2014
    Labeler - The Mentholatum Company (002105757)
    Registrant - The Mentholatum Company (002105757)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Mentholatum Company002105757manufacture(10742-0002)
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