Label: SECRET DIG WHITENING SUNSCREEN SPRAY. SPF50 PA- secret dig whitening sunscreen spray spf50 pa aerosol, spray

  • NDC Code(s): 84462-458-01
  • Packager: Yiwu Mijue electronic Commerce Co., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 9, 2024

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  • ACTIVE INGREDIENT

    HOMOSALATE

    OCTINOXATE

    OCTISALATE

  • PURPOSE

    A lightweight sunscreen spray specially designed foroutdoor use can effectively block the exposure of UVA andUVB,evenly cover the skin, with fresh texture, and can breapplied at any time.lt is fresh and not greasy, and can formsunscreen isolation layer on the surface of the skin to providesunscreen care.

  • INDICATIONS & USAGE

    A lightweight sunscreen spray specially designed for outdoor use can effectively block the exposure of UVA and UVB

    Usage:Shake well before use,10-15cm away from the skin and spray evenly on the skin exposed to sunlight(hands,legs,neck,back)

  • DOSAGE & ADMINISTRATION

    Store in a ventilated and dry environmen below 50 °c, avoid direct sunlight, and keep away from fire and heat sources.

    Net:150ml

  • KEEP OUT OF REACH OF CHILDREN

    Please keep out of reach of infants and young children

  • WARNINGS

    Warning:For external use only,please do not ch e mouh,nose or eyes,do not use in areas with skin damage inflammation or itching

  • INACTIVE INGREDIENT

    DECYL GLUCOSIDE

    BISOCTRIZOLE

    WATER

    DEHYDROXANTHAN GUM

    N-SALICYLOYLGLYCINE

    BEMOTRIZINOL

    ETHYLHEXYL TRIAZONE

    2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL

    OCTOCRYLENE

    ZINC OXIDE

    STEARIC ACID

  • PRINCIPAL DISPLAY PANEL

    22

  • INGREDIENTS AND APPEARANCE
    SECRET DIG WHITENING SUNSCREEN SPRAY. SPF50 PA 
    secret dig whitening sunscreen spray spf50 pa aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84462-458
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE36 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE36 g  in 100 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE20 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    BISOCTRIZOLE (UNII: 8NT850T0YS)  
    WATER (UNII: 059QF0KO0R)  
    DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)  
    N-SALICYLOYLGLYCINE (UNII: 5BR3P7J05U)  
    BEMOTRIZINOL (UNII: PWZ1720CBH)  
    ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)  
    2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL (UNII: 1ZRR9A405A)  
    OCTOCRYLENE (UNII: 5A68WGF6WM)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84462-458-01150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/27/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/27/2024
    Labeler - Yiwu Mijue electronic Commerce Co., LTD (413886387)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yiwu Mijue electronic Commerce Co., LTD413886387manufacture(84462-458) , label(84462-458)
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