Home > Drugs A-Z > Olay Complete All Day Moisturizer

Olay Complete All Day Moisturizer (Procter & Gamble Manufacturing Company)

Available Formats

Dosage Form Package Information Links
LOTION 1 BOTTLE, PLASTIC in 1 CARTON (37000-233-12) > 120 mL in 1 BOTTLE, PLASTIC Label Information
LOTION 1 BOTTLE, PLASTIC in 1 CARTON (37000-233-17) > 177 mL in 1 BOTTLE, PLASTIC Label Information

Complete Olay Complete All Day Moisturizer Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • ACTIVE INGREDIENT

    Active ingredients Purpose
    Octinoxate 6.0% Sunscreen
    Zinc Oxide 3.0% 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 product is 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 water resistant sunscreen if swimming or sweating
    • 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
    • children under 6 months: ask a doctor

  • Other information

    • protect this product from excessive heat and direct sun

  • Inactive ingredients

    water, glycerin, isohexadecane, polyacrylamide, C13-14 isoparaffin, laureth-7, cyclopentasiloxane, PEG/PPG-20/20 dimethicone, steareth-21, stearyl alcohol, sucrose polycottonseedate, behenyl alcohol, tocopheryl acetate, cetyl alcohol, DMDM hydantoin, iodopropynyl butylcarbamate, steareth-2, triethoxycaprylylsilane, disodium EDTA, aloe barbadensis leaf juice, oleth-3 phosphate.


  • Questions or comments?

    Call 1-800-285-5170


  • SPL UNCLASSIFIED SECTION

    Dist. by
    PROCTER & GAMBLE,
    CINCINNATI, OH 45202


  • PRINCIPAL DISPLAY PANEL - 177 mL Bottle Carton

    OLAY®

    complete
    all day moisturizer
    with sunscreen

    BROAD SPECTRUM SPF 15
    WITH VITAMIN E AND ALOE

    sensitive

    OIL-FREE

    6.0 FL OZ (177 mL)

    15

    PRINCIPAL DISPLAY PANEL - 177 mL Bottle Carton

  • INGREDIENTS AND APPEARANCE
    OLAY COMPLETE ALL DAY MOISTURIZER   BROAD SPECTRUM SPF 15 SENSITIVE
    octinoxate and zinc oxide lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-233
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 6 g  in 100 mL
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 3 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    glycerin (UNII: PDC6A3C0OX)  
    isohexadecane (UNII: 918X1OUF1E)  
    C13-14 isoparaffin (UNII: E4F12ROE70)  
    laureth-7 (UNII: Z95S6G8201)  
    cyclomethicone 5 (UNII: 0THT5PCI0R)  
    PEG/PPG-20/20 dimethicone (UNII: BA94B7CK8K)  
    steareth-21 (UNII: 53J3F32P58)  
    stearyl alcohol (UNII: 2KR89I4H1Y)  
    docosanol (UNII: 9G1OE216XY)  
    .alpha.-tocopherol acetate (UNII: 9E8X80D2L0)  
    cetyl alcohol (UNII: 936JST6JCN)  
    DMDM hydantoin (UNII: BYR0546TOW)  
    iodopropynyl butylcarbamate (UNII: 603P14DHEB)  
    steareth-2 (UNII: V56DFE46J5)  
    triethoxycaprylylsilane (UNII: LDC331P08E)  
    edetate disodium (UNII: 7FLD91C86K)  
    aloe vera leaf (UNII: ZY81Z83H0X)  
    oleth-3 phosphate (UNII: 8Q0Z18J1VL)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:37000-233-12 1 in 1 CARTON 05/01/2012 02/28/2018
    1 120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2 NDC:37000-233-17 1 in 1 CARTON 05/01/2012 02/28/2018
    2 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 05/01/2012 02/28/2018
    Labeler - Procter & Gamble Manufacturing Company (004238200)
    Establishment
    Name Address ID/FEI Business Operations
    The Procter & Gamble Manufacturing Company 017745779 MANUFACTURE(37000-233)