Label: ZAPRO HAND SANITIZER- hand sanitizer gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 26, 2020

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  • Active Ingredient(s)

    Ethyl Alcohol 94%

  • Purpose

    Antiseptic

  • Use

    Use
    for hand washing to decrease bacteria on he skin， only when water is not ava able

  • Warnings

    Flammable—Keep away from fire and flames
    For external use only

  • Do not use

    Do not get into eyes
    lf contact occurs， rinse thoroughly with water

  • When using this product

    When using this product
    Do not get into eyes
    lf contact occurs， rinse thoroughly with water

    Stop use and ask a doctor if
    Irritation and redness develop

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

  • STOP USE

    Stop use and ask a doctor if
    Irritation and redness develop

  • 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

    Press pump twice to dever two s quits of product on to the pam of your hand
    Rub hands together and allow to dry without wiping

  • Other information

    May discolor fabrics or surfaces
    Store below 110°F(43°C)

  • Inactive ingredients

    water, cellulosico-polymer, zinc pyrithione

  • Package Label - Principal Display Panel

    75209-011-01 250ml 75209-011-01 250ml

    75209-011-02 2000ml

    75209-011-02 2000ml

  • INGREDIENTS AND APPEARANCE
    ZAPRO HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75209-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL94 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5)  
    WATER (UNII: 059QF0KO0R)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75209-011-01250 mL in 1 BOTTLE; Type 0: Not a Combination Product06/22/2020
    2NDC:75209-011-022000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/22/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/22/2020
    Labeler - GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD. (546631081)
    Establishment
    NameAddressID/FEIBusiness Operations
    GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.546631081manufacture(75209-011)
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