Label: MOISTURE SURGE- cream cream

  • NDC Code(s): 83872-279-01
  • Packager: Shenzhen Xiaomai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 9, 2024

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  • Active ingredients

    Aloe Ferox Leaf Extract 2%
    Sodium Hyaluronate 1.5%

  • Purpose

    Moisturizes throughout theday & helps protects

  • Uses

    Apply sunscreen generously to exposedskin. Rub it in evenly. Reapply as neededespecially after swimming or sweating.

  • 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,Butylene Glycol,Propylene Glycol,Cetearyl Alcohol,Hyaluronic Acid,Xanthan Gum

  • PRINCIPAL DISPLAY PANEL

    LBEAL

  • INGREDIENTS AND APPEARANCE
    MOISTURE SURGE 
    cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-279
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A) (PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER - UNII:788QAG3W8A) PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER1 g  in 50 mL
    ALOE FEROX LEAF (UNII: 0D145J8EME) (ALOE FEROX LEAF - UNII:0D145J8EME) ALOE FEROX LEAF1 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-279-0150 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product07/09/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/09/2024
    Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xiaomai Manufacturing Co., Ltd.712999147manufacture(83872-279)
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