Label: GLIZA BODY MIST SUNSCREEN BROAD SPECTRUM SPF 100- sunscreen spray

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 19, 2020

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  • Active Ingredient(s)

    Avobenzone 3% 
    Homosalate 15% 
    Octisalate 5% 
    Octocrylene 10% 
    Oxybenzone 6% 

  • Purpose

    Sunscreen

  • Use

    Uses helps prevent sunburn if used as  directed with other sun protection measures decreases the risk of skin cancer
    and early skin aging caused by the sun.

  • Warnings

    For External Use Only. Flammable, keep away from fire, sparks, and source of
    ignition. Do not store above 110 oF

    When using this product:

    Keep out of eyes. In case of contact with eyes, ush thoroughly with water. Avoid contact
    with broken skin.


    Stop use and ask a doctor if irritation and redness develop and persist for more
    than 72h.


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

  • WHEN USING

    Directions :

    Spray liberally and spread evenly by hand 15 minutes before sun
    exposur apply to all skin exposed to the sun. Reapply after 80 minutes of
    swimming or sweating, immediately after towel drying. Reapply at least every
    2 hours. Children under 6 months of age:
    Ask a doctor

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • Inactive ingredients

    Ethyl Alcohol, Polyester-7 & Neopentyl Glycol Diheptanoate, Fragrance (Perfume),
    Glycerine, Aloe Barbadensis Leaf Juice, Propanediol, Tocopherol (Vitamin E)
    Phenoxyethanol, Ethylhexylglycerin,

  • Package Label - Principal Display Panel

    0.06 L (60 mL) NDC: 77903-002-01image description

  • INGREDIENTS AND APPEARANCE
    GLIZA BODY MIST SUNSCREEN BROAD SPECTRUM SPF 100 
    sunscreen spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77903-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1.8 mg  in 60 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE9 mg  in 60 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE3 mg  in 60 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE6 mg  in 60 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE3.6 mg  in 60 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    POLYESTER (ADIPIC ACID, 1,6-HEXANEDIOL, NEOPENTYL GLYCOL) (UNII: 571593769G)  
    FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    2-ETHYLHEXYL GLYCIDYL ETHER (UNII: LU1UZ98B89)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77903-002-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product05/19/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35205/19/2020
    Labeler - EMRA LLC (116584354)
    Registrant - EMRA LLC (116584354)
    Establishment
    NameAddressID/FEIBusiness Operations
    EMRA LLC116584354manufacture(77903-002)
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