Label: HAND SANITIZER WIPES- alcohol cloth

  • NDC Code(s): 75214-503-10, 75214-503-50, 75214-503-80
  • Packager: HANUL CO.,LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 9, 2024

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  • Active Ingredient(s)

    Ethyl Alcohol 75% Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer Wipes

  • Use

    To decrease bacteria on the skin that could cause disease

  • Warnings

    For external use only: hands

    Flammable. Keep away from fire and flame.

  • WHEN USING

    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

    Stop Use and ask a doctor if

    irritation or redness develops

    condition persists for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    • Wet hands thoroughly with product and allow to dry without wiping
    • Not recommended for infants
  • Other information

    do not store above 105ºF/40°C

    may discolor some fabrics

    harmful to wood finishes and plastics

  • Inactive ingredients

    water, glycerin, hydrogen peroxide

  • Package Label - Principal Display Panel

    rico

    hand sanitizing wipes

    non-sterile solution

    kills 99.9 of common illness-causing germs

    75% alcohol antiseptic

    80wipes

    10wipes

    rico hand sanitizer wipes

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75214-503
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL  in 100 mL
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL  in 100 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75214-503-50334 mL in 1 PACKAGE; Type 0: Not a Combination Product03/30/2020
    2NDC:75214-503-10134 mL in 1 PACKAGE; Type 0: Not a Combination Product03/30/2020
    3NDC:75214-503-80534 mL in 1 PACKAGE; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/30/2020
    Labeler - HANUL CO.,LTD (557814370)
    Establishment
    NameAddressID/FEIBusiness Operations
    HANUL CO.,LTD557814370manufacture(75214-503)
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