Label: ALL DAY MOISTURE- 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 April 11, 2022

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

View All Sections
  • Active ingredients

    Octinoxate 6.0%

    Zinc Oxide 3.0%

  • Purpose

    Sunscreen

  • Uses

    • helps prevent sunburn
    • if used as diected 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 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 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 as sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
    • limit time in the sun, espcially from 10 a.m. - 2 p.m.
    • wear long-sleeved shirts, pants, hats and sunclasses
    • children under 6 months of age: ask a doctor
  • Other information

    protect the product from excessive heat and direct sun

  • Inactive ingredients

    water, glycerin, isohexadecane, sodium acrylate/sodium acryloyldimethyl taurate copolymer, polysorbate 80, laureth-7, cylopentasiloxane, cyclohexasiloxane, PEG/PPG-20/20 dimethicone, steareth-21, stearyl alcohol, Gossypium Herbaceum (cotton) seed oil, behenyl alcohol, cetyl alcohol, DMDM hydantoin, iodopropynyl butylcarbamate, fragrance, tocopheryl acetate, disodium EDTA, steareth-2, oleth-3 phosphate, ascorbic acid, panthenol

  • claims

    TopCare

    beauty

    ALL-DAY

    MOISTURE LOTION

    For Normal Skin

    Light, non-greasyt formula

    Non-comedogenic

    (won't clog pores)

    Paraben Free

    Light, fast-absorbing

    moisture lasts all day

    Softens

    Smoothes for radiant skin

    ALL-DAY

    MOISTURE LOTION

    For Normal Skin

    ALL DAY MOISTURE

    Complete beauty lotion moisture for all day hydration.

    Formulated antioxidant vitamin E plus C and nourishing beauty moisture that absorbs quickly into skin and lasts all day to help your skin stay soft, smooth and beautiful

    UV PROTECTION

    Broad spectrum

    UVA and UVB protection with SPF 15 to help prevent premature skin damage.

  • SPL UNCLASSIFIED SECTION

    DISTRIBUTED BY TOPCO ASSOCIATES LLC

    ELK GROVE VILLAGE, IL 60007

    TOPCO VIJA1019

    QUESTIONS? 1-888-420139

    This product is not manufactured or distributed by Procter & Gamble, distributor of Olay Complete All Day Moisturizer with Sunscreen.

  • principal display panel

    TopCare

    beauty

    ALL-DAY

    MOISTURE LOTION

    For Normal Skin

    Compare to OLAY

    Broad spectrum SPF 15 sunscreen

    Dermatologist Tested

    SPF 15

    6 FL OZ (177mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ALL DAY MOISTURE 
    octinoxate, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-192
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate61.2 mg  in 1 mL
    Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION30.6 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    LAURETH-7 (UNII: Z95S6G8201)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    PEG/PPG-20/20 DIMETHICONE (UNII: BA94B7CK8K)  
    STEARETH-21 (UNII: 53J3F32P58)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    LEVANT COTTONSEED OIL (UNII: N5CFT140R8)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    STEARETH-2 (UNII: V56DFE46J5)  
    OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:36800-192-301 in 1 BOX02/05/2020
    1177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35202/05/2020
    Labeler - Topco (006935977)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(36800-192)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(36800-192)
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!