Label: SUPER CREME SOLAIRE CORPS BODY SUN CARE SPF 15- avobenzone, octinoxate, octisalate, oxybenzone cream

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

Drug Label Information

Updated November 30, 2023

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

View All Sections
  • Drug Facts

  • Active ingredients

    Avobenzone 3 % Octinoxate 5 % Octisalate 5 % Oxybenzone 4 %




    Purpose

    Sunscreen

  • Uses

    • 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.
  • 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

    if rash occurs.

    Keep out of reach of children.

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

  • Directions

    • Apply liberally 15 minutes before sun exposure.
    • Reapply at least every 2 hours.
    • Use a water resistant sunscreen if swimming or sweating.
    • Children under 6 months of age: ask a doctor.
    • Spending time in the sun increases your risk of skin cancer and early skin aging.  To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Sun Protection Measures: 
    • Limit time in the sun especially from 10 am to 2 pm.
    • Wear long-sleeved shirts, pants, hats, and sunglasses.
  • Other information

    Protect the product in this container from excessive heat or direct sun.

  • Inactive ingredients

    water, dipropylene glycol dibenzoate, butylene glycol, glycerin, butyrospermum parkii (shea butter), helianthus annuus (sunflower) seed oil, isodecyl neopentanoate, dimethicone, physalis alkekengi calyx extract, cetearyl alcohol, lauryl glucoside, polyglyceryl-2 dipolyhydroxystearate, phenoxyethanol, potassium cetyl phosphate, polyacrylamide, carbomer, elaeis guineensis (palm) oil, c13-14 isoparaffin, tocopheryl acetate, lavandula angustifolia (lavender) oil, sodium methyl paraben, allantoin, ceteareth-20, tetrasodium edta, pelargonium graveolens oil, sorbic acid, pentylene glycol, laureth-7, sodium hydroxide, citric acid, cetyl alcohol, bht, potassium sorbate, linalool, limonene, geraniol, citronellol, citral

  • PRINCIPAL DISPLAY PANEL

    SUPER CREME SOLAIRE CORPS  Body sun care   Sunscreen Cream  Broad Spectrum SPF 15  sisley PARIS  6.7 FL.OZ.  200 ml   Sisley USA  7 Renaissance Square, 3rd Floor, White Plains, NY 10601

  • PRINCIPAL DISPLAY PANEL

    b1Box 2Tube

    b2

  • INGREDIENTS AND APPEARANCE
    SUPER CREME SOLAIRE CORPS BODY SUN CARE   SPF 15
    avobenzone, octinoxate, octisalate, oxybenzone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66097-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIPROPYLENE GLYCOL DIBENZOATE (UNII: 6OA5ZDY41O)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SHEANUT OIL (UNII: O88E196QRF)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PHYSALIS ALKEKENGI CALYX (UNII: AL7F9NO9HR)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    PALM OIL (UNII: 5QUO05548Z)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)  
    ALLANTOIN (UNII: 344S277G0Z)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)  
    SORBIC ACID (UNII: X045WJ989B)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    LAURETH-7 (UNII: Z95S6G8201)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    GERANIOL (UNII: L837108USY)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    CITRAL (UNII: T7EU0O9VPP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66097-004-001 in 1 BOX01/21/2013
    1200 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/21/2013
    Labeler - C.F.E.B. Sisley (262279246)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!