Label: SUNSOLVE MD DETOX AND SHIELD- zinc oxide lotion

  • NDC Code(s): 84878-998-01, 84878-998-02
  • 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
  • Sunsolve MD Detox and Shield

    Dosage and Administration

  • Sunsolve MD Detox and Shield

    Inactive ingredients

  • Sunsolve MD Detox and Shield

    Indications & usage

  • Sunsolve MD Detox and Shield

    Active Ingredients

  • Sunsolve MD Detox and Shield

    keep out of reach of children

  • Sunsolve MD Detox and Shield

    purpose

  • Sunsolve MD Detox and Shield

    Warning Label

  • Sunsolve MD Detox and Shield

    PDP

  • INGREDIENTS AND APPEARANCE
    SUNSOLVE MD DETOX AND SHIELD 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84878-998
    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
    SCHINUS MOLLE OIL (UNII: 99O5U5NLK2)  
    JOJOBA OIL (UNII: 724GKU717M)  
    ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)  
    TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    COCO-CAPRYLATE (UNII: 4828G836N6)  
    NYLON-12 (UNII: 446U8J075B)  
    PHENYLPROPANOL (UNII: 0F897O3O4M)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)  
    .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)  
    POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)  
    STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
    CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84878-998-021 in 1 CARTON11/05/2024
    1NDC:84878-998-0148 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 DrugM02011/05/2024
    Labeler - Sunsolve MD Inc (119376976)
    Registrant - Nanophase Technologies Corporation (623502044)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanophase Technologies Corporation050383046api manufacture(84878-998)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanophase Technologies Corporation118812921pack(84878-998) , manufacture(84878-998)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanophase Technologies Corporation623502044manufacture(84878-998) , api manufacture(84878-998)
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!