Label: DR LIFT SUN CARE SPF 25- titanium dioxide, zinc oxide lotion

  • 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 March 21, 2023

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  • Active Ingredients

    Avobenzone 3.0%

    Homosalate 15.0%

    Octisalatae 5.0%

  • Purpose

    Sunscreen

  • Warnings

    Warnings

    • 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 immediately
  • Directions

    Directions: for sunscreen use

    . apply generously 15 minutes before sun exposure

    . apply to all skin exposed to the sun

    . children under 6 months of age: ask a doctor

  • Inactive Ingredients

    Inactive Ingredients: Aqua, SD Alcohol 40-B, Glycerin, Argania Spinosa Kernel Oil, Cetearyl Ethylhexanoate, Ammonium Polyacryloyldimethyl Taurate, Bisabolol, *CO Glycerin, Tocopheryl Acetate (Vitamin E), *CO Humulus Lupulus (Hops) Extract, *CO Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, *CO Calendula Officinalis Flower Extract, *CO Chamomilla Recutita (Matricaria) Flower Extract, *CO Citrus Limon (Lemon) Peel Extract, *CO Cucumis Sativus (Cucumber) Seed Extract, *CO Camellia Sinensis Leaf Extract, *CO Pyrus Malus (Apple) Fruit Extract, *CO Spirulina Platensis Extract, Phenoxyethanol, Ethylhexylglycerin.

    *CO - Certified Organic

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    Directions: for sunscreen use

    . apply generously 15 minutes before sun exposure

    . apply to all skin exposed to the sun

    . children under 6 months of age: ask a doctor

    Other information

    .protect the product in this container from excessive heat and direct sun

  • PRINCIPAL DISPLAY PANEL

    DrLiftSPF25_PRINT3aBOX

  • INGREDIENTS AND APPEARANCE
    DR LIFT SUN CARE SPF 25 
    titanium dioxide, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68062-8821
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE2.25 mg  in 45 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1.35 mg  in 45 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE6.75 mg  in 45 mL
    Inactive Ingredients
    Ingredient NameStrength
    ARGANIA SPINOSA SEED (UNII: 8H7X7XB54H)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68062-8821-125 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/21/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02003/21/2023
    Labeler - Spa de Soleil (874682867)
    Establishment
    NameAddressID/FEIBusiness Operations
    Spa de Soleil874682867manufacture(68062-8821)
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