Label: ALCOHOL PADS- ethyl alcohol cloth

  • 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 November 16, 2020

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  • SPL UNCLASSIFIED SECTION

    ALCOHOL Pads

  • Active Ingredient(s)

    Alcohol 1mL/pcs. Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Use

    ALCOHOL Pads 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

    • Wipe the surface of the skin and let it dry naturally.
    • 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

    Glycerol
    Dichlorbenzyl alcohol
    Propanedioi
    Triethanoiamine
    Purified water
    Carbomer

  • Package Label - Principal Display Panel

    0102

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PADS 
    ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81065-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    DICHLOROBENZYL ALCOHOL (UNII: 1NKX3648J9)  
    WATER (UNII: 059QF0KO0R)  
    10-(N-METHYLPIPERIDYLIDEN-4)-1-AZATHIOXANTHENE MALONATE (UNII: E6PD5WKQ63)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81065-101-0150 in 1 BOX; Type 0: Not a Combination Product11/17/2020
    2NDC:81065-101-02100 in 1 BOX; Type 0: Not a Combination Product11/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/17/2020
    Labeler - Jiangxi Jiemi Technology Co., Ltd. (715308233)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangxi Jiemi Technology Co., Ltd.715308233manufacture(81065-101)
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