Label: ALCOHOL WIPE- alcohol cloth

  • NDC Code(s): 79618-001-04
  • Packager: YAHON ENTERPRISE CO.,LTD
  • 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 December 21, 2022

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

View All Sections
  • Active Ingredient(s)

    Ethyl Alcohol 75% (alc/vol)

  • Purpose

    Antiseptic

  • Use

    Sanitizing wipes to help reduce bacteria on the skin or surface

  • Warnings

    Flammable, keep away from heat, spark, electrical fire or flame.

  • WHEN USING

    Avoid contact with eyes. If in eyes, remove contact lenses (if any), rinse slowly with water or get medical help.

  • STOP USE

    Stop use and ask a doctor if Irritation and redness develop or condition persists for more than 72 hours

    Ask a doctor before use if you have deep or puncture wounds, animal bites serious burns

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    Discard after single use and do not flush

  • Other information

    Do not apply internally. Store in a cool dry place below 30˚C

  • Inactive ingredients

    Water, Benzalkonium Chloride, Polyaminopropyl Biguanide, Citric Acid

  • Package Label - Principal Display Panel

    Comlete LabelPrincipal Display PanelDrug Facts50 wipes NDC: 79618-001-04

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPE 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79618-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79618-001-0450 in 1 PACKET; Type 0: Not a Combination Product07/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/11/2020
    Labeler - YAHON ENTERPRISE CO.,LTD (555347945)
    Establishment
    NameAddressID/FEIBusiness Operations
    YAHON ENTERPRISE CO.,LTD555347945manufacture(79618-001)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!