Label: SUNSOVLE MD VOLUMIZE AND RESTORE- zinc oxide lotion

  • NDC Code(s): 84878-823-01, 84878-823-02
  • Packager: Sunsolve MD Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2024

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

View All Sections
  • Sunsovle MD Volumize and Restore

    Dosage and Administration

  • Sunsovle MD Volumize and Restore

    Inactive ingredients

  • Sunsovle MD Volumize and Restore

    Indications & usage

  • Sunsovle MD Volumize and Restore

    Active Ingredients

  • Sunsovle MD Volumize and Restore

    keep out of reach of children

  • Sunsovle MD Volumize and Restore

    purpose

  • Sunsovle MD Volumize and Restore

    Warning Label

  • Sunsovle MD Volumize and Restore

    PDP

  • INGREDIENTS AND APPEARANCE
    SUNSOVLE MD VOLUMIZE AND RESTORE 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84878-823
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE110 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ETHYL STEARATE (UNII: C64RTC734W)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    SQUALANE (UNII: GW89575KF9)  
    ISODODECANE (UNII: A8289P68Y2)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    COCO-CAPRYLATE (UNII: 4828G836N6)  
    ETHYL OLEATE (UNII: Z2Z439864Y)  
    RUTIN (UNII: 5G06TVY3R7)  
    PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)  
    POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
    CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)  
    LIMNANTHES ALBA (MEADOWFOAM) SEED OIL (UNII: 412ZHA4T4Y)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    ETHYL PALMITATE (UNII: IRD3M534ZM)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    C13-15 ALKANE (UNII: 114P5I43UJ)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    ETHYL LINOLEATE (UNII: MJ2YTT4J8M)  
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84878-823-021 in 1 CARTON11/05/2024
    1NDC:84878-823-0150 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02011/05/2024
    Labeler - Sunsolve MD Inc (119376976)
    Registrant - Nanophase Technologies Corporation (623502044)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanophase Technologies Corporation050383046api manufacture(84878-823)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanophase Technologies Corporation118812921manufacture(84878-823) , pack(84878-823)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanophase Technologies Corporation623502044manufacture(84878-823) , api manufacture(84878-823)
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!