Label: CNP LABORATORY SUN CARE MILKY LIGHT SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 16, 2024

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

  • ACTIVE INGREDIENTS

    Avobenzone 2.7%
    Homosalate 9.0%
    Octisalate 4.5%
    Octocrylene 9.0%

  • PURPOSE

    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

    Do not use ​on damaged or broken skin

  • WHEN USING

    When using this product keep out of eyes. Rinse with water to remove.

  • STOP USE

    Stop use and ask doctor if rash occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    For sunscreen use:

    • apply liberally 15 minutes before sun exposure
    • children under 6 months of age: ask a doctor
    • 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 a 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

  • OTHER INFORMATION

    • protect the product in this container from excessive heat and direct sun
    • the product may stain certain types of fabrics
  • INACTIVE INGREDIENTS

    WATER, GLYCERIN, DIMETHICONE, CETEARYL ALCOHOL, ISODODECANE, POTASSIUM CETYL PHOSPHATE, ACRYLATES/POLYTRIMETHYLSILOXYMETHACRYLATE COPOLYMER, 1,2-HEXANEDIOL, BENZOTRIAZOLYL DODECYL P-CRESOL, PANTHENOL, GLYCERYL CAPRYLATE, GLYCERYL STEARATE, NIACINAMIDE, CAPRYLIC/CAPRIC TRIGLYCERIDE, MAGNESIUM ALUMINUM SILICATE, CETEARYL OLIVATE, INULIN LAURYL CARBAMATE, FRAGRANCE, SORBITAN OLIVATE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, XANTHAN GUM, DIPROPYLENE GLYCOL, TROMETHAMINE, TRISODIUM EDTA, MYRISTICA FRAGRANS (NUTMEG) EXTRACT, PAEONOL, PAEONIA SUFFRUTICOSA BRANCH/FLOWER/LEAF EXTRACT.

  • QUESTIONS?

    www.cnpmall.com

  • + Dermatologically tested

    + Dermatologically tested

    This sunsreen delivers superior
    broad spectrum protection against
    harmful UVB and UVA rays and
    provides skin care benefits. It con-
    tains panthenol and niacinamide,
    providing a moisturizing effect on
    the skin and helping to brighten
    the complexion. This lightweight
    formula is absorbed without any
    stickiness. Wear alone or under
    makeup.

    Questions?
    www.cnpmall.com

    MADE IN KOREA
    DISTR. LG H&H Co., Ltd.
    58, Saemunan-ro, Jongno-gu,
    Seoul, Korea

  • PRINCIPAL DISPLAY PANEL 50ml / 1.7 fl. oz Tube Carton

    CNP Laboratory

    SUN CARE

    MILKY
    LIGHT
    SUNSCREEN

    Broad Spectrum
    SPF 50

    50 ml / 1.7 fl. oz

    CNP Milky Light Sunscreen SPF50 OC

    CNP Milky Light Sunscreen SPF50 IC

  • INGREDIENTS AND APPEARANCE
    CNP LABORATORY SUN CARE MILKY LIGHT SUNSCREEN BROAD SPECTRUM SPF 50 
    avobenzone, homosalate, octisalate, octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53208-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 50 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE9 g  in 50 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2.7 g  in 50 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE9 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53208-101-501 in 1 CARTON02/16/2024
    150 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/16/2024
    Labeler - LG H&H Co.,Ltd. (688276187)
    Establishment
    NameAddressID/FEIBusiness Operations
    fmg Co.Ltd690188305manufacture(53208-101)