Label: ALLY HAND SANITIZER WIPES- alcohol cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 17, 2020

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Ethyl alcohol 70%

  • Purpose

    Antiseptic

  • Use

    to decrease bacteria on the skin

  • Warnings

    For external use only: hands

    Flammable. Keep away from heat and flame.

    When using this product

    • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
    • avoid contact with broken skin
    • do not inhale or ingest

    Stop use and ask a doctor if

    • irritation or redness develops
    • condition persists for more than 72 hours

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

  • Directions

    • wet hands thoroughly with the product and allow to dry without wiping
    • not recommended for infants
  • Other Information

    • do not store above 105°F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    Aloe barbadensis leaf juice, glycerin, isopropanol, propanediol, tocopheryl acetate, water

  • Questions?

    1-844-342-6691

  • PRINCIPAL DISPLAY PANEL - 20 Wipe Pouch

    ally®

    HAND
    SANITIZING WIPES

    Kills 99.99% of
    Germs Instantly*

    Fast and Effective
    70% Ethyl Alcohol

    Enriched with Moisturizers
    Aloe and Vitamin E

    037198R

    To Open Peel Back
    Resealable Label

    20 Wipes
    5.5in x 8.4in (13.9cm x 21.3cm)

    DO NOT FLUSH

    PRINCIPAL DISPLAY PANEL - 20 Wipe Pouch
  • INGREDIENTS AND APPEARANCE
    ALLY HAND SANITIZER WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50862-1310
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 29 mL
    ISOPROPYL ALCOHOL (UNII: ND2M416302) 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) 1 mL
    PROPANEDIOL (UNII: 5965N8W85T) 0.5 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.1 mL
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.001 mL
    Product Characteristics
    Color    Scoreno score
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50862-1310-420 in 1 POUCH; Type 0: Not a Combination Product04/05/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH DRUGM00304/05/2022
    Labeler - Guy & O'Neill, Inc. (037838844)
    Registrant - Guy & O'Neill, Inc. (037838844)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guy & O'Neill, Inc.037838844MANUFACTURE(50862-1310) , LABEL(50862-1310)
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