Label: ALCOHOL WIPES cloth

  • NDC Code(s): 75269-013-01, 75269-013-02, 75269-013-03, 75269-013-04, view more
    75269-013-05, 75269-013-06, 75269-013-07, 75269-013-08, 75269-013-09, 75269-013-10
  • Packager: LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 24, 2023

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  • Active ingredient(s)

    Alcohol 75%

  • Purpose

    Antiseptic

  • Warnings

    Do not use if you are allergic to alcohol, avoid contact with eyes.

    This product is disposable and cannot be reused.

    This product contains alcohol, away from sources of ignition, and should only be used outside the skin to avoid contact with the eyes. Do not allow infants to come into contact alone to avoid accidental ingestion.

    This product is insoluble in water, do no flush into the toilet.

    Keep out of reach of children. If swallowed, get medical help right away.

  • Warnings

    Keep out of reach of children. If swallowed, get medical help right away.

  • Other information

    Storage Method: Store in a cool place to avoid volatilization.

    Shelf Life: 2 years

  • Inactive ingredient(s)

    Water

  • Usage

    Open the sticker and then wipe.

  • Usage

    Open the sticker and then wipe.

  • Medicinal ingredient

    Ethyl alcohol (Ethanol) 75% v/v

  • Recommended use or purpose

    Antibacterial (skin) cleanser.

    Effective in destroying (harmful) bacteria to provide antiseptic cleansing.

    Kills (harmful) bacteria/germs.

  • Cautions and warnings

    Keep away from open flame and sources of heat.

    For external use only.

    Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

    Stop use and ask/consult a doctor/physician/health care practitioner/health care provider/health care professional if irritation develops.

    When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

  • Duration of use Recommended dosage

    Children, adolescents and adults 2 years and over

  • Directions for use

    For occasional and personal domestic use.

    Rub thoroughly into hands for at least 30 seconds. Allow to dry.

    Supervise children when they use this product.

  • Non-Medical Ingredient

    Water

  • Package Label

    ALCOHOL WIPES

    10PCS

    NDC: 75269-013-01 10 pcs label

    Package Label

    ALCOHOL WIPES

    1PCS

    1 pcs label

    ALCOHOL WIPES

    20 bags in a carton

    NDC: 75269-013-02 20 in carton label

  • Package Label

    ALCOHOL WIPES

    80PCS

    NDC: 75269-013-03 80 pcs label

  • Package Label

    ALCOHOL WIPES

    15PCS

    NDC: 75269-013-04 15pcs label

  • Package Label

    ALCOHOL WIPES

    50PCS

    NDC: 75269-013-05 50pcs label

  • Package Label

    ALCOHOL WIPES

    60PCS

    NDC: 75269-013-06 60pcs label

  • Package Label

    ALCOHOL WIPES

    100PCS

    NDC: 75269-013-07 100pcs label

  • Package Label

    ALCOHOL WIPES

    500PCS

    NDC: 75269-013-08 500pcs blank label

  • Package Label

    ALCOHOL WIPES

    80 Sheets

    NDC: 75269-013-09

    80 sheets label

  • PRINCIPAL DISPLAY PANEL

    ALCOHOL WIPES

    50 wipes

    NDC: 75269-013-10

    Label required by client

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPES 
    alcohol wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75269-013
    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
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75269-013-0110 in 1 BAG03/27/2020
    14 mL in 1 PATCH; Type 0: Not a Combination Product
    2NDC:75269-013-0220 in 1 CARTON03/27/2020
    24 mL in 1 BAG; Type 0: Not a Combination Product
    3NDC:75269-013-0380 in 1 BAG03/27/2020
    34 mL in 1 PATCH; Type 0: Not a Combination Product
    4NDC:75269-013-0415 in 1 BAG03/27/2020
    44 mL in 1 PATCH; Type 0: Not a Combination Product
    5NDC:75269-013-0550 in 1 BAG03/27/2020
    54 mL in 1 PATCH; Type 0: Not a Combination Product
    6NDC:75269-013-0660 in 1 BAG03/27/2020
    64 mL in 1 PATCH; Type 0: Not a Combination Product
    7NDC:75269-013-07100 in 1 BAG03/27/2020
    74 mL in 1 PATCH; Type 0: Not a Combination Product
    8NDC:75269-013-08500 in 1 CANISTER03/27/2020
    84 mL in 1 PATCH; Type 0: Not a Combination Product
    9NDC:75269-013-0980 in 1 CANISTER03/27/2020
    94 mL in 1 PATCH; Type 0: Not a Combination Product
    10NDC:75269-013-1050 in 1 BAG03/27/2020
    104 mL in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/27/2020
    Labeler - LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD. (560972943)
    Registrant - LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD. (560972943)
    Establishment
    NameAddressID/FEIBusiness Operations
    LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD.560972943manufacture(75269-013)
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