Label: PREQUEL SKIN UTILITY GEL MULTI-PURPOSE SKIN PROTECTANT- skin protectant gel gel

  • NDC Code(s): 82800-050-01
  • Packager: The Center Brands, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 30, 2023

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

View All Sections
  • Purpose

    Skin Protectant

  • Active Ingredients

    Glycerin 20%

  • Uses

    Temporarily protects and helps releive chafed, chapper or cracked skin

    Helps protect fomr the drying effects of wind and cold weather

  • Warnings

    Fox external use only.

    When using this product do not get into eyes

    Stop use and ask a doctor if condition worsens

    symptoms last more than 7 days or clear up and occur again within a few days

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Apply as needed.

  • Inactive ingredients

    Water (Aqua), Dimethicone, Panthenol, PEG/PPG/18 Dimethicone Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Tuarate Copolymer, Panthenyl Triacetate, Niacinamide, Naringenin, C15-23 Alkane, 1,2 Hexanediol, C13-14 Alkcane, Phenoxyethanol, Decyl Glucoside, Tetrasodium Glutamate Diacetate, Citric Acid, Sodium Hydroxide.

  • Other Information

    • protect the product in this container from excessive
    heat and direct sun

  • Questions?

    Visit prequelskin.com

  • Principal Display Panel

    82800-050-01

  • INGREDIENTS AND APPEARANCE
    PREQUEL SKIN UTILITY GEL MULTI-PURPOSE SKIN PROTECTANT 
    skin protectant gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82800-050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
    PANTHENYL ETHYL ETHER ACETATE (UNII: S2FA5ZM21C)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    NARGENICIN (UNII: XP2QP458K4)  
    C15-23 ALKANE (UNII: J3N6X3YK96)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82800-050-011 in 1 PACKAGE10/30/2023
    150 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01610/30/2023
    Labeler - The Center Brands, LLC (076228814)
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!