Label: DR. EASY INSTANT HAND SANITIZING WIPES- 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 September 2, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol, 75%

    purpose

    Antiseptic

  • Use

    For sanitizing hands to decrease bacteria on the skin.

  • Warnings:

    Flammable, keep away from fire or flame. For external use only.

    When using this product

    Keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

    Stop use and ask a doctor

    If significant irritation, or sensitization develops. Consult a physician if irritation persists for more than 5 days

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Peel back label at tab remove wipes as needed. reseal pouch by pressing label firmly back into place. wipe hands thoroughly with product.allow hands to air dry. Discard after single use.

  • Other information

    Do not store above 105F

  • Inactive ingredients

    Aloe barbadensis leaf juice (aloe vera), fragrance, glycerin, propylene glycol, water.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    DR. EASY INSTANT HAND SANITIZING WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52056-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52056-000-3030 in 1 BAG06/30/2020
    13 mL in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/30/2020
    Labeler - Dr. Easy Bio-Tech (Hefei) Co., Ltd. (529687751)
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