Label: HERS MINERAL SUNSCREEN MULTI-SCREEN- zinc oxide lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 March 7, 2023

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  • hers mineral sunscreen multi-screen

    PDP

  • INGREDIENTS AND APPEARANCE
    HERS MINERAL SUNSCREEN MULTI-SCREEN 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71730-901
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE132 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHENYLPROPANOL (UNII: 0F897O3O4M)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ISOAMYL LAURATE (UNII: M1SLX00M3M)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    CETETH-20 (UNII: I835H2IHHX)  
    PULLULAN (UNII: 8ZQ0AYU1TT)  
    SQUALANE (UNII: GW89575KF9)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    CYCLODEXTRINS (UNII: 7E6SK9QDT8)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71730-901-021 in 1 CARTON10/04/2021
    1NDC:71730-901-0130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35210/04/2021
    Labeler - HIMS (080678637)
    Registrant - Nanophase Technologies Corporation (623502044)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanophase Technologies Corporation118812921manufacture(71730-901) , pack(71730-901)