Label: DAYLOGIC TINTED DAILY MOISTURIZER SPF 30- ensulizole, octinoxate, oxybenzone, zinc oxide lotion

  • Category: HUMAN OTC DRUG LABEL

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 14, 2017

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  • Active ingredients

    Ensulizole 2%

    Octinoxate 7.5%

    Oxybenzone 6%

    Zinc Oxide 5%

    Purpose

    Sunscreen

  • Uses

    • helps prevent sunburn
    • if used as directed with other sun protectio 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.

    Sto 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

    ​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 sun, especially from 10 a.m. - 2 p.m.
    • wear long-sleeved shirts, pants, hats, and sunglasses
    • apply liberally 15 minutes before sun exposure
    • use a water resistant sunscreen if swimming or sweating
    • reapply at least every 2 hours
    • children under 6 months: ask a doctor
  • Other information

    protect this product from excessive heat and direct sun.

  • Inactive ingredients

    Water (Aqua), C12-15 Alkyl Benzoate, Caprylyl Methicone, Glcerin, Cetearyl Alcohol, Isohexadecane, Trimethylolpropane Triethylhexanoate, PEG-100 Stearate, Glyceryl Stearate, Butyloctyl Salicylate, Triethanolamine, Calcium Pantothenate, Bisabolol, Dicetyl Phosphate, Ceteth-10 Phosphate, Propylene Glycol, Butylene Glycol, Codium Tomentosum Extract, Caprylic/Capric Triglyceride, Sodium Acrylates Copolymer, Xanthan Gum, Phenoxyethanol, Methylparaben, Ethylparaben, Propylparaben, Isobtuylparaben, Butylparaben, Iron Oxides (CI 77491, CI 77492, CI 77499).

  • Questions or comments?

    1-866-695-3030

  • Label copy

    Image of the label

  • INGREDIENTS AND APPEARANCE
    DAYLOGIC TINTED DAILY MOISTURIZER SPF 30 
    ensulizole, octinoxate, oxybenzone, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-3430
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE20 mg  in 1 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE60 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION50   in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    TRIMETHYLOLPROPANE TRIETHYLHEXANOATE (UNII: B952ZGW1IL)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    CALCIUM PANTOTHENATE (UNII: 568ET80C3D)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
    CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CODIUM TOMENTOSUM (UNII: B8B45BRU87)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    SODIUM ACRYLATE (UNII: 7C98FKB43H)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-3430-150 mL in 1 TUBE; Type 0: Not a Combination Product08/13/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35208/13/2017
    Labeler - Rite Aid Corporation (014578892)
    Registrant - Apollo Health and Beauty Care Inc. (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care Inc.201901209manufacture(11822-3430)