Label: ULINE HAND SANITIZER- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 18, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active Ingredient

    Active Ingredient

    Ethyl Alcohol 70%

  • Uses

    Uses

    • Hand sanitizer to reduce microorganisms on the skin.

    • Use this product when soap and water are not available.

  • Purpose

    Purpose

    Antiseptic

  • Warnings

    Warnings

    • For external use only.

    • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    • FLAMMABLE. This product contains ethyl alcohol. Keep away from

    sources of ignition.

    • Discontinue use if irritation or redness develops.

    • If irritation persists for more than 72 hours, consult a physician.

    • KEEP OUT OF REACH OF CHILDREN.

    • If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Directions

    • Read the entire label before using this product.

    • Place enough product on your palm to thoroughly cover your hands.

    • Rub hands together briskly until dry.

  • Inactive Ingredients

    Inactive Ingredients

    Water, PEG/PPG-8/3 Laurate, Gycerin, Carbomer, Tetrahydroxypropylethylendiamine, Fragrance.

  • Warnings

    KEEP OUT OF REACH OF CHILDREN.

  • Principal Display Panel

    3780 ml label3780 ml 69790-801-04

  • INGREDIENTS AND APPEARANCE
    ULINE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69790-801
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    DIMETHICONE PEG-8 LAURATE (UNII: 72MF9C2A18)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EDETOL (UNII: Q4R969U9FR)  
    ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X)  
    OCTOXYNOL-13 (UNII: 480KVF3EBY)  
    CYCLOHEXANE (UNII: 48K5MKG32S)  
    HEXYL SALICYLATE (UNII: 8F78EY72YL)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    LINALOOL (UNII: D81QY6I88E)  
    NEROL (UNII: 38G5P53250)  
    .GAMMA.-TERPINENE (UNII: 4YGF4PQP49)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    .ALPHA.-PINENE (UNII: JPF3YI7O34)  
    ALLYL CYCLOHEXANEPROPIONATE (UNII: H4W9H3L241)  
    GERANIOL (UNII: L837108USY)  
    CITRONELLOL (UNII: P01OUT964K)  
    PROPYLENE OXIDE (UNII: Y4Y7NYD4BK)  
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69790-801-043780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/08/2020
    Labeler - Uline (039612668)
    Registrant - Betco Corporation, Ltd (005050158)
    Establishment
    NameAddressID/FEIBusiness Operations
    Betco Corporation, Ltd005050158manufacture(69790-801) , label(69790-801)
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

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!