Label: ADOYA SANITIZING WIPES LEMONGRASS SCENT- 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 12, 2020

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  • Drug Facts

  • Active ingredient

    Alcohol 70%

    Purpose

    Antiseptic

  • Use

    For hand washing to decrease bacteria on the skin.

  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    Do not use

    in the eyes

    Stop use and ask a doctor if

    • irritation or redness develop
    • condition persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

  • Other information

    • Store in cool and dry place, away from direct sunlight
    • Close the lid to maintain quality and cleanliness
    • Do not use as a diaper wipe
    • Do not flush down the toilet
  • Inactive ingredients

    Purified water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Benzalkonium Chloride, Aloe vera, PEG 40 Hydrogenated Castor oil, Lemongrass extract.

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    ADOYA SANITIZING WIPES LEMONGRASS SCENT 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79708-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CYMBOPOGON CITRATUS LEAF (UNII: 06JMS448M5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79708-002-015 in 1 BAG10/02/2020
    15.79 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/02/2020
    Labeler - Jokki Labs LLC (117570400)
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