Label: KEYS SOULCARE DAILY MOISTURIZER BROAD SPECTRUM SPF30 SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene cream

  • NDC Code(s): 76354-442-01, 76354-442-02, 76354-442-03
  • Packager: e.l.f. Cosmetics, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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

View All Sections
  • Drug Facts

  • Active ingredients

    Avobenzone 3.0%

    Homosalate 9.0%

    Octisalate 5.0%

    Octocrylene 7.0%

    Purpose

    Sunscreen

  • Use

    • 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.
  • Warning

    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 doctorif:

    rash occurs.

    Keep out of reach of children.

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

  • Directions

    • Apply libreally 15 minutes before sun exposure, Reapply at least every 2 hours.
    • Use water resistant sunscreen if swimming or sweating.
    • 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 Braod Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in sun, especially from 10 a.m.-2 p.m., wear long-sleeved shirts, pants, hats and sunglasses. Children under 6 months of age: ask a doctor. Sun Protection Measures:
  • Other Information

    • Protect the product in this container from excessive heat and direct sun.
  • Inactive Ingredients

    Water (Aqua), Glycerin, Polyglyceryl-3 Distearate, Niacinamide, Aluminum Starch Octenylsuccinate, Trehalose, Silica, Stearyl Heptanoate, Phenoxyethanol, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Chamomilla Recutita (Matricaria) Flower Water, Panthenol, Squalane, Butylene Glycol, Stearic Acid, Palmitic Acid, Cetearyl Olivate, Sorbitan Olivate, Cetearyl Alcohol, Glyceryl Stearate Citrate, Stearyl Caprylate, Dimethicone, Polyacrylate Crosspolymer-6, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Coco-Glucoside, Carbomer, Caprylyl Glycol, Ethylhexylglycerin, Disodium EDTA

  • Questions or comments?

    1-888-315-9814

  • Package Labeling:50 mL

    Label

  • Package Labeling:15 mL

    Label2

  • Package Labeling:5 mL

    Label3

  • INGREDIENTS AND APPEARANCE
    KEYS SOULCARE DAILY MOISTURIZER BROAD SPECTRUM SPF30 SUNSCREEN 
    avobenzone, homosalate, octisalate, octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-442
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE90 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    TREHALOSE (UNII: B8WCK70T7I)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARYL HEPTANOATE (UNII: 2M4UGL1NCN)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)  
    PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)  
    CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SQUALANE (UNII: GW89575KF9)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)  
    STEARYL CAPRYLATE (UNII: 06TS6O9194)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76354-442-011 in 1 CARTON04/30/2022
    150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:76354-442-021 in 1 CARTON04/30/2022
    215 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:76354-442-031 in 1 CARTON04/30/2022
    35 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02004/30/2022
    Labeler - e.l.f. Cosmetics, Inc (093902816)
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!