Label: SHIMMER OIL- avobenzone homosalate octisalate octocrylene oil

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 16, 2024

If you are a consumer or patient please visit this version.

  • Dosage and Administration

    Apply liberally 15 minutes before sun exposure

    Reapply at least every 2 hours

    Use a water resistant sunscreen if swimming or sweating

  • 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 is rash occurs

  • Indications and Usage

    Helps prevent sunburn

    If used as directed 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

    In case of ingestion, get medical help or contact a Poison Control Center right away

  • Purpose

    Sunscreen

  • Inactives

    Argania Spinosa Kernel Oil, Bisabolol, Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Oil, Calcium Sodium Borosilicate

    Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Seed Oil, Cocos Nucifera (Coconut) Oil, Dextrin Palmitate, Dimethicone, Ethyl Ferulate, Fragrance, Hyaluronic Acid, Iron Oxides, Mica, Musa Sapientum (Banana) Fruit Extract, Neopentyl Glycol, Diethylhexanoate, Palmitoyl Tripeptide-1, Sclerocarya Birrea Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Titanium Dioxide

    Tocopherol, Trimethylpentanediol/Adipic Acid/Glycerin Crosspolymer

  • Vacation Shimmer Oil

    Shimmer Body Oil

  • INGREDIENTS AND APPEARANCE
    SHIMMER OIL 
    avobenzone homosalate octisalate octocrylene oil
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80641-015
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2.9 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE8 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.9 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80641-015-1586 mL in 1 BOTTLE; Type 0: Not a Combination Product03/07/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/07/2024
    Labeler - Vacation Inc. (117644631)