Label: BIOMATE MULTI-PURPOSE ALCOHOL WIPES- alcohol cellular sheet

  • Category: HUMAN OTC DRUG LABEL

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 October 20, 2020

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  • SPL UNCLASSIFIED SECTION

    This is a multi-purpose alcohol wipes manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

    The multi-purpose alcohol wipes is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

    1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
    2. Glycerol (1.45% v/v).
    3. Hydrogen peroxide (0.125% v/v).
    4. Sterile distilled water or boiled cold water.

    The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

  • Active Ingredient(s)

    Alcohol 80% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    Multi-purpose alcohol wipes to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
    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 or rash occurs. These may be signs of a serious condition.

  • 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

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
  • Inactive ingredients

    glycerin, hydrogen peroxide, purified water USP

  • Package Label - Principal Display Panel

    175 ml package label NDC: 80560-002-02175 ml NDC 80560-002-02

    192 ml label NDC:80560-002-01

    192 ml NDC 80560-002-01

    240 ml cannister label NDC:80560-002-03

    240 ml NDC 80560-002-03

    360 ml label NDC: 80560-002-04360 ml NDC: 80560-002-04

    384 ml NDC: 80560-002-05384 ml NDC: 80560-002-05

    480 ml NDC: 80560-002-06480 ml NDC: 80560-002-06

    960 ml NDC: 80560-002-07480 ml NDC: 80560-002-07

  • INGREDIENTS AND APPEARANCE
    BIOMATE MULTI-PURPOSE ALCOHOL WIPES 
    alcohol cellular sheet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80560-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL  in 100 mL
    WATER (UNII: 059QF0KO0R)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80560-002-01192 mL in 1 CANISTER; Type 0: Not a Combination Product08/06/2020
    2NDC:80560-002-02175 mL in 1 PACKAGE; Type 0: Not a Combination Product08/06/2020
    3NDC:80560-002-03240 mL in 1 CANISTER; Type 0: Not a Combination Product08/06/2020
    4NDC:80560-002-04360 mL in 1 CANISTER; Type 0: Not a Combination Product08/06/2020
    5NDC:80560-002-05384 mL in 1 CANISTER; Type 0: Not a Combination Product08/06/2020
    6NDC:80560-002-06480 mL in 1 CANISTER; Type 0: Not a Combination Product08/06/2020
    7NDC:80560-002-07960 mL in 1 CANISTER; Type 0: Not a Combination Product08/06/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/06/2020
    Labeler - KYB KUYUMCULUK INSAAT TURIZM GIDA ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI (365680187)
    Establishment
    NameAddressID/FEIBusiness Operations
    KYB KUYUMCULUK INSAAT TURIZM GIDA ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI365680187manufacture(80560-002)
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