Label: MENTHOLATUM NATURAL ICE ORIGINAL- dimethicone, octinoxate, octisalate ointment

  • NDC Code(s): 10742-3004-1, 10742-3004-2, 10742-3004-3, 10742-3004-4, view more
    10742-3004-8, 10742-3004-9
  • 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

    Dimethicone 1%

    Octinoxate 7.5%

    Octisalate 5%

  • Purpose

    Dimethicone - Skin protectant

    Octinoxate - Sunscreen

    Octisalate - Sunscreen

  • Uses

    • helps prevent sunburn
    • temporarily protects chapped or cracked lips
  • Warnings

    Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging.

    For external use only

    Do not use

    on damaged or broken skin

    When using this product

    keep out of eyes. Rinse with water to remove.

    Stop use and ask a doctor if

    • rash occurs
    • condition worsens
    • symptoms last 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

    • apply liberally 15 minutes before sun exposure
    • use a water resistant sunscreen if swimming or sweating
    • reapply at least every 2 hours
    • children under 6 months: ask a doctor

    Other information

    • protect this product from excessive heat and direct sun
  • Inactive ingredients

    mineral oil, ozokerite, petrolatum, lanolin, fragrance, menthol

  • Questions?

    1-877-636-2677

    MON-FRI 9AM to 5PM (EST)

    mentholatum.com

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  • INGREDIENTS AND APPEARANCE
    MENTHOLATUM NATURAL ICE  ORIGINAL
    dimethicone, octinoxate, octisalate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-3004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE10 mg  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    CERESIN (UNII: Q1LS2UJO3A)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    LANOLIN (UNII: 7EV65EAW6H)  
    LEVOMENTHOL (UNII: BZ1R15MTK7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10742-3004-11 in 1 BLISTER PACK01/19/199904/01/2019
    14.5 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:10742-3004-94.5 g in 1 TUBE; Type 0: Not a Combination Product01/19/199904/01/2019
    3NDC:10742-3004-21 in 1 BLISTER PACK04/02/2019
    34.2 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:10742-3004-84.2 g in 1 TUBE; Type 0: Not a Combination Product04/02/2019
    5NDC:10742-3004-31 in 1 BLISTER PACK01/19/1999
    54.5 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:10742-3004-44.5 g in 1 TUBE; Type 0: Not a Combination Product01/19/1999
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/19/1999
    Labeler - The Mentholatum Company (002105757)
    Registrant - The Mentholatum Company (002105757)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Mentholatum Company002105757manufacture(10742-3004)
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