Label: 20 PACK ALCOHOL HAND WIPES-ALOE cloth

  • 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 September 23, 2020

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  • Active Ingredient(s)

    Ethanol Alcohol 75% v/v. Purpose: Antibacterial

  • Purpose

    Antibacterial

  • Use

    Decreases bacteria on skin.

  • Warnings

    • For external use only.
    • Keep away from fire or flame
  • When using

    When using this product keep out of eyes. If contact with eyes occurs, rinse thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation or rash appears and lasts.

  • Do not use

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    • Wet hands thoroughly with product and allow to dry.
    • Children under 6 years of age should be supervised when using product.
  • Other information

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

    Water, Fragrance.

  • Package Label - Principal Display Panel

    20 CLOTH IN 1 PACKAGE NDC: 75163-021-20

    20 CLOTH LABEL

  • INGREDIENTS AND APPEARANCE
    20 PACK ALCOHOL HAND WIPES-ALOE 
    20 pack alcohol hand wipes-aloe cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75163-021
    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
    ALOE (UNII: V5VD430YW9)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75163-021-2020 in 1 PACKAGE09/08/2020
    14 mL in 1 PATCH; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/08/2020
    Labeler - Zhuji Jianhe Paper Co., Ltd (554529241)
    Registrant - Zhuji Jianhe Paper Co., Ltd (554529241)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhuji Jianhe Paper Co., Ltd554529241manufacture(75163-021)
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