Label: CARNUS HAND SANITIZER WIPES- 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 August 19, 2020

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  • Drug Facts

  • Active ingredient[s]

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Use[s] :

    Hand sanitizer wipes 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 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.

  • Directions :

    • Unfold wipe; Wipe hands; Discard after use.

    • 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 :

    Water, Ethylhexylglycerin, Hydroxy Ethyl Cellulose, N-alkyl ethylbenzyl dimethyl ammonium chloride, Phenoxyethanol.

  • SPL UNCLASSIFIED SECTION

    70 % ALCOHOL

    KILLS 99,9% OF GERMS

    FRAGRANCE FREE

    MANUFACTURED BY:

    DINAMO KOZMETIK VE TEKSTIL DIS TICARET A.S.

    AYOSB MERMERCILER CAD. NO: 10

    AYDINLI / TUZLA / ISTANBUL / TURKEY

    www.dinamogrup.com

    EN 14476:2013+A2:2019

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    CARNUS HAND SANITIZER WIPES 
    ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79853-105
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79853-105-5050 in 1 BOX08/18/2020
    11 in 1 PACKET
    13 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/18/2020
    Labeler - DINAMO KOZMETIK VE TEKSTIL DIS TICARET ANONIM SIRKETI (533088658)
    Establishment
    NameAddressID/FEIBusiness Operations
    DINAMO KOZMETIK VE TEKSTIL DIS TICARET ANONIM SIRKETI533088658manufacture(79853-105)
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