Label: WET WIPES cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated May 31, 2020

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

  • Active Ingredient(s)

    Alcohol, Benzalkonium Chloride, C12-14-Alkyldimethyl(Ethylbenzyl) Ammonium Chlorides, Ethylhexylglycerin, Chlorphenesin

  • Purpose

    Antiseptic, disinfection and surface cleaning

  • Use

    TO disinfect and deodorize hard, nonporous surfaces.

  • Warnings

    Back of Package

  • Do not use

    Do not use or store near heat or open flame.

  • WHEN USING

    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.

  • STOP USE

    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

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

  • Directions

    back

  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
    • Do not use or store near open heat or flame.
  • Inactive ingredients

    glycerin, purified water, fragrance

  • PRINCIPAL DISPLAY PANEL

    Front of Package

    Package Label - Principal Display Panel

    80 wipes

    NDC 7663-101-45

  • INGREDIENTS AND APPEARANCE
    WET WIPES 
    wet wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76693-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM (UNII: 7N6JUD5X6Y) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM0.06 g  in 100 g
    PHENOXYETHANOL (UNII: HIE492ZZ3T) (PHENOXYETHANOL - UNII:HIE492ZZ3T) PHENOXYETHANOL0.3 g  in 100 g
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA) DIDECYLDIMONIUM CHLORIDE0.4 g  in 100 g
    CHLORPHENESIN (UNII: I670DAL4SZ) (CHLORPHENESIN - UNII:I670DAL4SZ) CHLORPHENESIN0.1 g  in 100 g
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.1 g  in 100 g
    WATER (UNII: 059QF0KO0R) 48.97 g  in 100 g
    FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK) 0.02 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76693-101-4580 g in 1 PACKAGE; Type 5: Device Coated or Otherwise Combined with Biologic07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/15/2020
    Labeler - Sourcery Ltd (800787645)
    Registrant - Sourcery Ltd (800787645)