Label: ZEROSWEAT WITH ALOE- antiperspirant liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 June 28, 2021

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  • ACTIVE INGREDIENT

    Aluminum Chloride 12% ... Antiperspirant

  • PURPOSE

    Antiperspirant

  • KEEP OUT OF REACH OF CHILDREN

    WARNING: Keep out of reach of children.

  • INDICATIONS & USAGE

  • INDICATIONS & USAGE

    Reduces underarm perspiration.

  • INACTIVE INGREDIENT

    Purified Water, Glycerin (Skin Emollient), Allantoin, Chamomile Flower Extract, Aloe Barbadensis Leaf Juice, Salix Alba “Willow” Bark Extract (Botanical Extract Blend), Sodium Bicarbonate.

  • WARNINGS

    For external use only.

    Do not use:

    • Immediately after shaving
    • Immediately after bathing
    • On irritated skin
    • On broken skin

    Stop use if rash occurs
    Ask a doctor before use if you have kidney disease

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

  • DOSAGE & ADMINISTRATION

    Apply to the appropriate body area.

    Apply only at bedtime

    Apply sparingly

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ZEROSWEAT WITH ALOE 
    antiperspirant liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65112-259
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE0.12 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 0.85 g  in 1 g
    ALLANTOIN (UNII: 344S277G0Z) 0.005 g  in 1 g
    GLYCERIN (UNII: PDC6A3C0OX) 0.02 g  in 1 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65112-259-0128.35 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product03/14/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35003/14/2019
    Labeler - I Shay Cosmetics Inc (151582384)
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