Label: COMPLETE BEAUTY- octinoxate, 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 July 28, 2017

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

  • Claims

    daylogic

    complete

    beauty lotion

    BROAD SPECTRUM SPF 15

    SUNSCREEN

    MOISTURIZER

    SPF 15

    Close
  • Active ingredient

    Octinoxate 6.0%

    Zinc oxide 3.0%

    Close
  • Purpose

    Sunscreen

    Close
  • 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
    Close
  • Warnings

    For external use only

    Close
  • Do Not Use

    on damaged or broken skin

    Close
  • When using this product

    keep out of eyes. Rinse with water to remove.

    Close
  • Stop use and ask a doctor if

    rash occurs

    Close
  • Keep out of reach of children

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

    Close
  • Directions

    • apply liberally 15 minutes before sun exposure
    • reapply at least every 2 hours
    • use a 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
    • limit time in the 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
    Close
  • Other information

    • protect the product from excessive heat and direct sun
    Close
  • Inactive ingredients

    water, glycerin, isohexadecane, polysorbate 80, sodium acrylate/acryloyldimethyl taurate copolymer, laureth-7, cyclopentasiloxane, PEG/PPG-20/20 dimethicone, steareth-21, stearyl alcohol, gossypium herbaceum (cotton) seed oil, behenyl alcohol, tocopheryl acetate, cetyl alcohol, DMDM hydantoin, iodopropynyl butylcarbamate, steareth-2, disodium EDTA, aloe barbadensis leaf extract, oleth-3 phosphate,

    Close
  • side panel claims

    complete

    beauty lotion

    BROAD SPECTRUM SPF 15

    SUNSCREEN

    MOISTURIZER

    SPF 15

    Close
  • Adverse Reactions

    Distributed by rite Aid

    30 Hunter Lane

    Camp Hill, PA 17011

    Close
  • Disclaimer

    This product is not manufactured or distributed by Procter & Gamble, distributor of Olay Complete All Day Moisturer Lotion

    Close
  • ADVERSE REACTION SECTION

    DISTRIBUTED BY: RITE AID

    30 HUNTER LANE,

    CAMP HILL, PA 17011

    MADE IN THE U.S.A. WITH U.S. AND FOREIGN COMPONENTS

    look great

    feel great

    100% GUARANTEE

    or your money back

    503.001/503AA

    Close
  • Principal Display Panel

    daylogic 

    complete

    beauty lotion

    BROAD SPECTRUM SPF 15

    SUNSCREEN MOISTURIZER

    SPF 15

    DERMATOLOGITS

    TESTED

    Sensitive Skin

    UVA/UVB Protection

    Vitamin E & Aloe

    Compare to Olay Complete

    All Day Moisture Lotion

    6 FL OZ (177 mL)

    image description

    Close
  • INGREDIENTS AND APPEARANCE
    COMPLETE BEAUTY 
    octinoxate, zinc oxide lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0091
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 30 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
    LAURETH-7 (UNII: Z95S6G8201)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PEG/PPG-20/20 DIMETHICONE (UNII: BA94B7CK8K)  
    STEARETH-21 (UNII: 53J3F32P58)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    LEVANT COTTONSEED OIL (UNII: N5CFT140R8)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    STEARETH-2 (UNII: V56DFE46J5)  
    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:11822-0091-6 1 in 1 CARTON 03/13/2010
    1 177 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 final part352 03/13/2010
    Labeler - Rite Aid (014578892)
    Registrant - Vi-Jon (790752542)
    Establishment
    Name Address ID/FEI Business Operations
    Vi-Jon 790752542 manufacture(11822-0091)
    Close