Label: ZEROSWEAT ANTIPERSPIRANT 12%- antiperspirant lotion

  • NDC Code(s): 65112-306-01, 65112-306-02
  • Packager: I. Shay Cosmetics
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 13, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Aluminum Chloride- 12%

  • PURPOSE

    Antiperspirant

  • KEEP OUT OF REACH OF CHILDREN

    WARNING: Keep out of reach of children

  • INDICATIONS & USAGE

    Decreases excessive perspiration.

    Decreases underarm sweating.

  • INACTIVE INGREDIENT

    Purified Water, Aloe Vera Extract, Allantoin, Willow Bark Extract, Chamomile Extract, Glycerin, Sodium Bicarbonate.

  • WARNINGS

    For External Use Only.

    Ask a doctor before use if you have kidney disease.

    Do not use:

    -Immediately after shaving

    -On irritated skin

    -On broken skin

    -Immediately after bathing

    When using this product do not use in or near eyes.

    Stop use and ask doctor if rash or irritation develops

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Apply to appropriate body area. Apply sparingly. Apply only a few strokes under each arm. Apply only at bedtime.

  • PRINCIPAL DISPLAY PANEL

    Zero Sweat antiperspirant

  • INGREDIENTS AND APPEARANCE
    ZEROSWEAT ANTIPERSPIRANT 12% 
    antiperspirant lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65112-306
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE0.12 g  in 35.5 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65112-306-021 in 1 BOX06/01/2024
    1NDC:65112-306-0135.5 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01906/01/2024
    Labeler - I. Shay Cosmetics (151582384)
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

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!