Label: FACE SUNSCREEN SKIN CARE- face sunscreen cream

  • NDC Code(s): 83872-012-01
  • Packager: Shenzhen Xiaomai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 28, 2024

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

View All Sections
  • Active ingredients

    Octinoxate 5%
    Octocrylene 5%
    Zinc oxide 6.2%

  • Purpose

    Sunscreen
    Moisturizes throughout theday & helps protects

  • Uses

    Apply sunscreen generously to exposedskin. Rub it in evenly. Reapply as neededespecially after swimming or sweating.Enjoy your sun-protected day!

  • Wamings

    For exteral use only

  • Do not use

    on damaged or broken skin

  • When using this product

    Only for external use. do not ingest.
    Avoid direct contact with eyes.

  • 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.

  • Ask Doctor

    When Pregnant or breast-feeding.

  • Directions

    Directions for use
    -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 a B road.
    -Spectrum SPF value of15 or higher and other sun protection：
    -limit time in the sun, especially from 10 a.m.-2 p.m.
    -and wear long-sleeved shirts, pants, hats, and sunglasses

  • Other information

    Before use, read all information on thecarton Store at controlled room temperature20 to 25 C (68 to 77°F)

  • Inactive ingredients

    Water, Glycerin, Cetearyl Alcohol, Butylene Glycol,Niacinamide, Sodium Hyaluronate, Tocopherol, Centella,Asiatica Extract,Camellia Sinensis Leaf Extract,Ethylhexylglycerin, Carbomer, Triethoxycaprylyisilane,Phenoxyethanol,Xanthan Gum,Additional Ingredients(Fragrances,Stabilizers,etc.),Dibutyl Adipate,Polymethylsiisesquioxane,Coco-Caprylate/Caprate,Hyaluronic Acid.

  • PRINCIPAL DISPLAY PANEL

    labellabellabellabellabel

  • INGREDIENTS AND APPEARANCE
    FACE SUNSCREEN SKIN CARE 
    face sunscreen cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE5 g  in 100 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE6.2 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)  
    1,3-BUTYLENE GLYCOL 1-PROPIONATE (UNII: 17U77WTV66)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-012-0150 g in 1 BOTTLE; Type 0: Not a Combination Product01/29/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/29/2024
    Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xiaomai Manufacturing Co., Ltd.712999147manufacture(83872-012)
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!