Label: EXUVIANCE AGE REVERSE DAY REPAIR WITH SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, octinoxate, and octisalate cream

  • NDC Code(s): 58414-0023-1
  • Packager: NeoStrata Company Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 August 31, 2023

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Avobenzone 3%
    Octinoxate 7.5%
    Octisalate 5%

  • 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

    Stop use and ask a doctor if rash occurs

    When using this product keep out of eyes. Rinse with water to remove.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

    A light peeling or tingling sensation may occur when using this high strength formulation. If uncomfortable, reduce usage to every other day until skin adjusts.

  • Directions

    • Apply liberally to face and neck daily following cleansing, 15 minutes before sun exposure
    • Use a water resistant sunscreen if swimming or sweating
    • Reapply at least every 2 hours
    • Sun Protection Measures. 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:
      • Limit time in the sun, especially from 10 am – 2 pm
      • Wear long-sleeved shirts, pants, hats and sunglasses
    • Children under 6 months: Ask a doctor
  • Other information

    • Store at 15°C-30°C (59°F – 86°F)
    • Protect this product from excessive heat and direct sun
  • Inactive ingredients

    Water, Acetyl Glucosamine, Butyloctyl Salicylate, Cyclopentasiloxane, Glyceryl Stearate, Butylene Glycol, Butyrospermum Parkii (Shea) Butter, PEG-100 Stearate, Dimethicone, Cetyl Alcohol, Nylon-12, Triacontanyl PVP, Retinol, Citric Acid, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Coffea Arabica (Coffee) Fruit Extract, Tocopheryl Acetate, Rosa Damascena Flower Oil, Punica Granatum Extract, Arginine, Glycerin, Propylene Glycol, Cyclohexasiloxane, Caprylyl Glycol, Dimethiconol, Disodium EDTA, BHT, Xanthan Gum, PEG-75 Stearate, Ceteth-20, Steareth-20, Polysorbate 20, Triethyl Citrate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Methyldihydrojasmonate, Carbomer, Ethylene Brassylate, Phenoxyethanol, Chlorphenesin, Yellow 5 (CI 19140), Red 33 (CI 17200).

  • Questions or comments?

    Call toll-free 1-800-225-9411 (9am – 5pm ET)

  • PRINCIPAL DISPLAY PANEL - 50 g Tube Carton

    exuviance®

    BELIEVE

    comprehensive
    antiaging

    AGE REVERSE
    DAY REPAIR
    WITH SUNSCREEN
    BROAD SPECTRUM SPF 30
    Protect, even skin tone
    Reduce the appearance
    of lines and wrinkles
    Retinol
    NeoGlucosamine
    Antioxidants
    Net Wt 50 g/1.75 oz

    Principal Display Panel - 50 g Tube Carton
  • INGREDIENTS AND APPEARANCE
    EXUVIANCE AGE REVERSE DAY REPAIR   WITH SUNSCREEN BROAD SPECTRUM SPF 30
    avobenzone, octinoxate, and octisalate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58414-0023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    N-ACETYLGLUCOSAMINE (UNII: V956696549)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    NYLON-12 (UNII: 446U8J075B)  
    TRICONTANYL POVIDONE (UNII: N0SS3Q238D)  
    RETINOL (UNII: G2SH0XKK91)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)  
    PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)  
    PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)  
    COFFEA ARABICA FRUIT (UNII: HOX6BEK27Q)  
    ROSA X DAMASCENA FLOWER OIL (UNII: 18920M3T13)  
    ARGININE (UNII: 94ZLA3W45F)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    PEG-75 STEARATE (UNII: OT38R0N74H)  
    CETETH-20 (UNII: I835H2IHHX)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58414-0023-11 in 1 CARTON10/01/2019
    150 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart35210/01/2019
    Labeler - NeoStrata Company Inc. (605754829)