Label: CLEANZ ECO BAMBOO WIPES- wipes cloth

  • NDC Code(s): 83061-001-01, 83061-001-02, 83061-001-03
  • Packager: McF Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 27, 2023

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  • ACTIVE INGREDIENT

    Active Ingredient

    Benzalkonium Chloride 0.13%w/w

  • PURPOSE

    Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Specially formulated for:

    Gyms and Fitness Centers

    Schools and Offices

    Yoga & Dance Studios

    Beauty Centers and Massage Therapy Spas

  • WARNINGS

    Warnings

    ·If eye contact occurs, rinse thoroughly with water.

    ·If irritation and redness persists, seek medical help.

    ·Keep out of the reach of children and pets. Do NOT use as baby wipes.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children and pets. Do NOT use as baby wipes

  • DOSAGE & ADMINISTRATION

    Directions:

    ·Do not remove the gym wipes from the bag or they'll dry out

    ·Cut a small V-shaped opening in the center of the bag

    ·Place the bag with the roll into the dispenser

    ·Pull sheet up through dispenser

    ·Dispense wipes by pulling up and tearing off

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Aqua, Phenoxyethanol, Glycerin, Disodium Cocoamphodiacetate, Polysorbate 20, Aloe Barbadensis Leaf Juice, Benzoic Acid, Potassium Sorbate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Menthol and Sodium Citrate.

  • STORAGE AND HANDLING

    Other information

    ·Store between 15-30C(59-86F)
    ·Avoid freezing and excessive heat above 40C (104F)

  • PRINCIPAL DISPLAY PANEL

    NDC: 83061-001-01

    Product Label Updated 1025

  • PRINCIPAL DISPLAY PANEL

    NDC: 83061-001-02

    1000 Sheets Label

  • PRINCIPAL DISPLAY PANEL

    NDC: 83061-001-03

    1500 sheets label

  • INGREDIENTS AND APPEARANCE
    CLEANZ ECO BAMBOO WIPES 
    wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83061-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MENTHOL (UNII: L7T10EIP3A)  
    ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83061-001-01900 in 1 PACKAGE10/15/2022
    10.00468 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:83061-001-021000 in 1 PACKAGE10/15/2022
    20.00468 g in 1 POUCH; Type 0: Not a Combination Product
    3NDC:83061-001-031500 in 1 PACKAGE10/15/2022
    30.00468 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/15/2022
    Labeler - McF Holdings LLC (075197605)
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