Label: SOFT FOCUS CITY SUNCREEN SERUM BROAD SPECTRUM SPF 30 SUPERGOOP- avobenzone, homosalate, octisalate, octocrylene liquid

  • NDC Code(s): 70157-005-01, 70157-005-02
  • Packager: Baxter Laboratories Pty. Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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 November 22, 2022

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  • ACTIVE INGREDIENT

    Active Ingredients         Purpose

    Avobenzone 3%            Sunscreen

    Homosalate 8%            Sunscreen

    Octisalate 4%               Sunscreen

    Octocrylene 2%            Sunscreen  

  • PURPOSE

    Uses Helps prevent sunburn

    If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer snd early skin aging caused by the sun

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • 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.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    Apply two pumps to face and neckat least 15 minutes prior to sun exposure. Oil-free and fast absorbing, it's ideal for use alone or as a smoothing primer under the rest of your skincare regimen.  Use a water resistant sunscreen if swimming or sweating

    Reapply at least every 2 hours

    Children under 6 months: Ask a doctor

  • INACTIVE INGREDIENT

    Inactive Ingredients Aqua, Cyclopentasilosiloxane, Isostearyl Neopentanoate, Glycerin, Cyclohexasiloxane, Ceteareth-20, Polypropylene, Cetearyl Alcohol, Caprylyl Glycol, Xanthan Gum, PEG-40 Stearate, Triacontanyl PVP, Silica, Ammonium Acryloyldimethyltaurate/VP Copolymer, Panthenyl Triacetate, Cetyl Dimethicone, Ethyl Linoleate, Caprylhydroxamic Acid, Oleyl Alcohol, Tocopherol, Disodium EDTA, Panthenol, Triethanolamine, Pentylene Glycol, Sodium Lactate, Lactic Acid, Serine, Urea, Sorbitol, Sodium Chloride, Allantoin, CI 77492, CI77491, CI77499

  • PRINCIPAL DISPLAY PANEL

    Supergoop!

    City Sunscreen Serum With vitamins E & B5

    Broad Spectrum SPF 30

    Soft Focus Finish

    Lightweight, Anti-aging Serum moisturizes and repairs while protecting from premature photoaging

    1.7 fl. oz. / 60 ml

    image description

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    Secondary

  • INGREDIENTS AND APPEARANCE
    SOFT FOCUS CITY SUNCREEN SERUM BROAD SPECTRUM SPF 30  SUPERGOOP
    avobenzone, homosalate, octisalate, octocrylene liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70157-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE8 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    PANTHENOL TRIACETATE, (+)- (UNII: 1206E8961B)  
    CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
    ETHYL LINOLEATE (UNII: MJ2YTT4J8M)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    OLEYL ALCOHOL (UNII: 172F2WN8DV)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    SERINE (UNII: 452VLY9402)  
    UREA (UNII: 8W8T17847W)  
    SORBITOL (UNII: 506T60A25R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ALLANTOIN (UNII: 344S277G0Z)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PEG-40 STEARATE (UNII: ECU18C66Q7)  
    TRICONTANYL POVIDONE (UNII: N0SS3Q238D)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70157-005-021 in 1 CARTON12/30/2014
    1NDC:70157-005-0160 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02012/30/2014
    Labeler - Baxter Laboratories Pty. Ltd. (740537709)
    Registrant - Baxter Laboratories Pty. Ltd. (740537709)
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