Label: ADOYA 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 August 7, 2020

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredient

    Ethyl 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 ue and ask a doctor if

    • irritation and 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

    2-Bromo-2-Nitropropane-1,3-Diol, Aloe Vera, Disodium Cocoamphodiacetate, Glycerin, Lemon extract, PEG-40 Hydrogenated Castor oil, Water.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    ADOYA SANITIZING WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79708-001
    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
    BRONOPOL (UNII: 6PU1E16C9W)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LEMON (UNII: 24RS0A988O)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79708-001-015 in 1 BAG08/07/2020
    114 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 finalpart333E08/07/2020
    Labeler - Jokki Labs LLC (117570400)