Label: NEXGEN SUNSCREEN BROAD SPECTRUM SPF 36 DOC MARTINS- octinoxate, oxybenzone, octocrylene, avobenzone cream

  • NDC Code(s): 56152-5010-1
  • Packager: Cosmetic Enterprises Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 19, 2023

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  • ACTIVE INGREDIENT

    ​Active Ingredients:                           Purpose:

    Octinoxate 7.0% Benzophenone-3    ​Sunscreen

    (Oxybenzone) 5.0% Octocrylene 4.0% Avobenzone 3.0%

  • PURPOSE

    ​Uses:

    Helps prevent sunburn. If used as described with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

  • KEEP OUT OF REACH OF CHILDREN

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

  • INDICATIONS & USAGE

    Stop use and ask a doctor if rash occurs.

  • WARNINGS

    ​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.

  • DOSAGE & ADMINISTRATION

    ​Directions:

    - Apply liberally 15 minutes before sun exposure.

    - Reapply after 80 minutes of swimming or sweating, immediately after towel drying, at least every 2 hours.

    - Children under 6 months: ask a doctor.

  • INACTIVE INGREDIENT

    Beeswax, Caprylic/Capric Triglyceride, Cetyl Alcohol, Cetyl Dimethicone, Cetyl Lactate, Cpernicia Cerifera (Carnauba) Wax, C10-30 Cholesterol/Lanosterol, Euphorbia Cerifera (Candelilla) Wax, Fragrance, Neopentyl Glycol Diheptanoate, Phenoxyethanol, Polybutene, Propylene Carbonate, Propylene Glycol Dibenzoate, Sea Whip Extract, Silica, Stearalkonium Hectorite

  • PRINCIPAL DISPLAY PANEL

    Doc Martin's of Maui

    NexGen Sunscreen

    New Skin Bonding Technology

    Broad Spectrum SPF 36

    Water Resistant (80 minutes)

    2.0 FL OZ (60 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    NEXGEN SUNSCREEN BROAD SPECTRUM SPF 36  DOC MARTINS
    octinoxate, oxybenzone, octocrylene, avobenzone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56152-5010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7 g  in 100 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE5 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE4 g  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    C10-30 CHOLESTEROL/LANOSTEROL ESTERS (UNII: 137SL7IL0Y)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    PROPYLENE GLYCOL DIBENZOATE (UNII: EQY32Z1AN4)  
    PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56152-5010-160 mL in 1 TUBE; Type 0: Not a Combination Product03/21/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/21/2017
    Labeler - Cosmetic Enterprises Ltd. (017701475)
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