Label: ALCOHOL WIPES 75% 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 28, 2020

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

View All Sections
  • Active Ingredient(s)

    ETHANOL ALCOHOL 75%

  • Purpose

    Antiseptic

  • Use

    SINGLE USE WIPES TO ClEAN & REMOVEA LLERGENS.

  • Warnings

    FOR EXTERNAL USE ONLY.

    DO NOT REPLACE WIIPES USED FOR MEDICAL PROCEDURES. THESE

    WIPES ARE MEANT FOR GENERAL CLEANSING.

    FLAMMABLE KEEP AWAY FROM FIRE OR FLAME. IF EYES CONTACT

    OCCURS, FLUSIH EYES WITH WATER.

    STORE AT ROOM TEMPERATURE 59F - 86F.

  • KEEP OUT OF REACH OF CHILDREN

    ·Keep out of reach of crildren.lf swallowed get medical help or contact a Poison Control Center right away.

  • WHEN USING

    When using this product avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.

    Stop use and ask a doctor if irritation and redness develop and persist.

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

  • Do not use

    DO NOT REPLACE WIIPES USED FOR MEDICAL PROCEDURES. THESE

    WIPES ARE MEANT FOR GENERAL CLEANSING.

  • STORAGE AND HANDLING

    STORE AT ROOM TEMPERATURE 59F - 86F.

  • Inactive ingredients

    WATER, ALOE VERA EXTRACT,HONEVSUCKLE EXTRACT

  • DOSAGE & ADMINISTRATION

    FLAMMABLE KEEP AWAY FROM FIRE OR FLAME. IF EYES CONTACT OCCURS, FLUSIH EYES WITH WATER.

  • STOP USE

    STOP USE: IF IRRITATION AND REDNESS DEVELOP. IF C·ONDITl10N CONTINUES, CONSULT YOUR HEALTH CARE PRACTITIONER.

  • Package Label - Principal Display Panel

    42129-018-01 50P

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPES 75% 
    alcohol wipes 75% cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42129-018
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    LONICERA HYPOGLAUCA WHOLE (UNII: V0QHS0RH24)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42129-018-0150 in 1 BAG; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/30/2020
    Labeler - Fustin (Xiamen) Commodity Co., Ltd. (421291161)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fustin (Xiamen) Commodity Co., Ltd.421291161manufacture(42129-018)
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!