Label: COMPLEXION PROTECTION MOISTURIZER SPF- benzophenone, avobenzone, octinoxate, octisalate cream cream

  • NDC Code(s): 70809-1902-1, 70809-1902-2
  • Packager: USRX LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 19, 2023

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  • PRINCIPAL DISPLAY PANEL

    .05 oz

    1.7 oz

    ACTIVE INGREDIENT -

    Benzophenone 3.6%

    Avobenzone 1%

    Octinoxate 7.5%

    Octisalate 5%

    Sunscreen

    FOR EXTERNAL USE ONLY

    DO NOT USE - On damaged or broken skin

    STOP USE AND ASK A DOCTOR IF A RASH OCCURRS

    Aqua (Water), Caprylic/Capric Triglyceride, Corn Starch Modified, Cetearyl Olivate, Diethylhexyl 2,6-Naphthalate, C12-15 Alkyl Benzoate, Sorbitan Olivate, Gluconolactone, Squalane, Glycerin, Cyclopentasiloxane, Tocopheryl Acetate (D-alpha), Sodium Hyaluronate (L), Xanthan Gum, Carbomer, Aminomethyl Propanol, Sodium Benzoate, Phenethyl Alcohol, Caprylyl Glycol, Phenoxyethanol, Trisodium Ethylenediamine Disuccinate, Potassium Sorbate​

  • INGREDIENTS AND APPEARANCE
    COMPLEXION PROTECTION MOISTURIZER SPF 
    benzophenone, avobenzone, octinoxate, octisalate cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70809-1902
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 mg  in 100 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 mg  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1 mg  in 100 mL
    BENZOPHENONE (UNII: 701M4TTV9O) (BENZOPHENONE - UNII:701M4TTV9O) BENZOPHENONE3.6 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    WATER (UNII: 059QF0KO0R)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SQUALANE (UNII: GW89575KF9)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70809-1902-150 mL in 1 TUBE; Type 0: Not a Combination Product07/08/2019
    2NDC:70809-1902-212 mL in 1 TUBE; Type 0: Not a Combination Product02/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02007/08/2019
    Labeler - USRX LLC (115270633)
    Registrant - USRX LLC (115270633)
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