Label: 75% ALCOHOL WIPES- alcohol wipes patch

  • NDC Code(s): 76641-101-01, 76641-101-10, 76641-101-25, 76641-101-31, view more
    76641-101-35
  • Packager: FuYang YangYang Health Technology Co. Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 25, 2024

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

View All Sections
  • Active ingredient

    Alcohol, 75% v/v, antiseptic

  • Inactive ingredient

    Water

  • Purpose

    Daily Clean for daily items and Antimicrobial.

  • When using

    This product is used to wipe hands, faces, skins, etc. It can also be used to clean many kinds of places.

  • Do not use

    Do not use in or contact the eyes.

  • Stop use

    Discontinue use if irritation and redness develop.

    If the condition persists for more than 72 hours, consult a physician.

  • Keep out of reach of children

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poision Control Center immediately.

  • Indications & usage

    This product is used to wipe hands, faces, skins, etc. It can also be used to clean many kinds of places.

    Open the label, take out the wet towel and wipe the target area.

  • Dosage & administration

    Use it as needed, after following the usage instructions.

    For external use only.

  • Warnings

    • For external use only.
    • THESE WIPES DO NOT REPLACE WIPES USED FOR MEDICAL PROCEDURES. THESE WIPES ARE MEANT FOR GENERAL CLEAN.

  • Other information

    • Keep in a dry place away from fire.
    • Please close the lid after dispensing to maintain purity. Alcohol by nature evaporates quickly.
  • Package label. Principal display panel

    label

  • INGREDIENTS AND APPEARANCE
    75% ALCOHOL WIPES 
    alcohol wipes patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76641-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 U  in 1 U
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeFREEFORMSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76641-101-1010 U in 1 PACKAGE; Type 0: Not a Combination Product05/05/2020
    2NDC:76641-101-011 U in 1 PACKAGE; Type 0: Not a Combination Product06/02/2020
    3NDC:76641-101-2550 U in 1 PACKAGE; Type 0: Not a Combination Product06/02/2020
    4NDC:76641-101-3180 U in 1 PACKAGE; Type 0: Not a Combination Product06/02/2020
    5NDC:76641-101-35100 U in 1 PACKAGE; Type 0: Not a Combination Product06/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/05/2020
    Labeler - FuYang YangYang Health Technology Co. Ltd (529735460)
    Registrant - FuYang YangYang Health Technology Co. Ltd (529735460)
    Establishment
    NameAddressID/FEIBusiness Operations
    FuYang YangYang Health Technology Co. Ltd529735460label(76641-101) , manufacture(76641-101)
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!