Label: MENTHOLATUM NATURAL ICE SPORT SPF 30- avobenzone, dimethicone, octinoxate, octisalate ointment

  • NDC Code(s): 10742-8980-1, 10742-8980-2, 10742-8980-3, 10742-8980-4, view more
    10742-8980-5, 10742-8980-6
  • Packager: The Mentholatum Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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  • Active ingredients

    Avobenzone 3%

    Dimethicone 1%

    Octinoxate 7.5%

    Octisalate 5%

  • Purpose

    Avobenzone - Sunscreen

    Dimethicone - Skin protectant

    Octinoxate - Sunscreen

    Octisalate - Sunscreen

  • Uses

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

    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
    • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
    • limit time in the sun, especially from 10 a.m. – 2 p.m.
    • wear long-sleeve shirts, pants, hats, and sunglasses
    • children under 6 months: ask a doctor

    Other information

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

    mineral oil, ozokerite, petrolatum, tricaprin, fragrance, aloe barbadensis leaf extract, cocos nucifera (coconut) oil, cholecalciferol, menthol, retinyl palmitate, tocopheryl acetate, zea mays (corn) oil

  • Questions?

    1-877-636-2677

    MON-FRI 9 AM to 5 PM (EST)

    mentholatum.com

  • Principal Display Panel

    Natural Ice Sport
  • Principal Display Panel

    Drug Facts
  • INGREDIENTS AND APPEARANCE
    MENTHOLATUM NATURAL ICE  SPORT SPF 30
    avobenzone, dimethicone, octinoxate, octisalate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8980
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    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)  
    TRICAPRIN (UNII: O1PB8EU98M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    CALCIFEDIOL (UNII: P6YZ13C99Q)  
    LEVOMENTHOL (UNII: BZ1R15MTK7)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    CORN OIL (UNII: 8470G57WFM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10742-8980-11 in 1 BLISTER PACK03/29/200004/01/2019
    14.5 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:10742-8980-24.5 g in 1 TUBE; Type 0: Not a Combination Product03/29/200004/01/2019
    3NDC:10742-8980-31 in 1 BLISTER PACK04/02/2019
    34.2 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:10742-8980-44.2 g in 1 TUBE; Type 0: Not a Combination Product04/02/2019
    5NDC:10742-8980-51 in 1 BLISTER PACK03/29/2000
    54.5 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:10742-8980-64.5 g in 1 TUBE; Type 0: Not a Combination Product03/29/2000
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/29/2000
    Labeler - The Mentholatum Company (002105757)
    Registrant - The Mentholatum Company (002105757)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Mentholatum Company002105757manufacture(10742-8980)
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