Label: CLOROX HEALTHCARE ALOEGUARD ANTIMICROBIAL- chloroxylenol liquid

  • NDC Code(s): 69540-0027-1, 69540-0027-2, 69540-0027-3, 69540-0027-4
  • Packager: Brand Buzz LLC
  • 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 February 2, 2023

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  • Active ingredient

    Chloroxylenol 0.75% w/w

  • Purpose

    Antiseptic

  • Uses

    • for hand-washing to decrease microbes on the skin
    • ideal for daily repeated washings
  • Warnings

    For external use only

  • WHEN USING

    When using this product

    • do not use in or near eyes
    • discontue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • Directions

    • wet hands
    • apply product (palmful)
    • wash hands vigorously
    • rinse thoroughly
  • Other information

    • store at room temperatuure
    • for healthcare professional use only
  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Cocamide MEA, Coco-Betaine, Coconut Fatty Acid, D&C Green No. 8, FD&C Blue No. 1, FD&C Yellow No. 5, Fragrance, Glycerin, Hydroxypropyl Methylcellulose, Monoethanolamine, Oleic Acid, Propylene Glycol Sodium Sulfate, Tetrasodium EDTA, Water.

  • Package Label: 118ml/532ml/798ml/3785ml

    CLOROX

    HEALTHCARE

    AloeGuard

    Does Not Contain Bleach

    Formerly

    AloeGuard

    from HealthLink

    Antimcrobial Soap

    Principal Display Panel Label

  • INGREDIENTS AND APPEARANCE
    CLOROX HEALTHCARE ALOEGUARD ANTIMICROBIAL 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69540-0027
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.75 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    COCO-BETAINE (UNII: 03DH2IZ3FY)  
    D&C GREEN NO. 8 (UNII: I2W85YOX9L)  
    OLEIC ACID (UNII: 2UMI9U37CP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    COCONUT ACID (UNII: 40U37V505D)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MONOETHANOLAMINE (UNII: 5KV86114PT)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69540-0027-1118 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/2021
    2NDC:69540-0027-2532 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/2021
    3NDC:69540-0027-43785 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/2021
    4NDC:69540-0027-3798 mL in 1 BAG; Type 0: Not a Combination Product04/20/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/20/2021
    Labeler - Brand Buzz LLC (079266204)
    Registrant - Brand Buzz LLC (079266204)
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