Label: XERAC AC liquid

  • NDC Code(s): 0096-0709-35, 0096-0709-60
  • Packager: Person and Covey
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2024

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  • OTC - PURPOSE SECTION

    For topical application as an antiperspirant (anhidrotic).

  • DOSAGE & ADMINISTRATION SECTION

    Xerac AC when applied to the underarms, should be applied to absolutely dry skin. Only apply Xerac AC before bedtime, since medication should be kept on the skin for 6-8 hours. To reduce irritation, let the alcohol evaporate, leaving a thin film of antiperspirant on the skin. Wear a T-shirt, while sleeping to prevent medication from being rubbed off on the bed linens. Do not apply Xerac AC to broken, irritated or recently shaved skin. Wash the treated area next morning with soap and water. Do not apply other deodorants or antiperspirants while using Xerac AC.

  • WARNINGS SECTION

    For external use only. Avoid contact with eyes. If contact occurs, wash eyes thoroughly with water. If irritation or sensitization occurs, discontinue use or contact a physician. Xerac AC may be harmful to cotton fibers and certain metals.

  • OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

  • OTC - ACTIVE INGREDIENT SECTION

    Aluminum Chloride Hexahydrate

  • INACTIVE INGREDIENT SECTION

    Anhydrous ethanol

  • Indicatins and Usage Section

    For patients suffering from hyperhidrosis, or patients whose jobs or sports activities cause excessive sweating that exacerbates other skin problems.

  • Principal Display Panel

    Xerac AC 35ccXerac AC 60cc

  • INGREDIENTS AND APPEARANCE
    XERAC AC 
    xerac ac liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0096-0709
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE0.0625 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0096-0709-6049.86 g in 1 PACKAGE; Type 0: Not a Combination Product06/01/1996
    2NDC:0096-0709-3529.09 g in 1 PACKAGE; Type 0: Not a Combination Product06/01/1996
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01906/01/1996
    Labeler - Person and Covey (008482473)
    Establishment
    NameAddressID/FEIBusiness Operations
    Person and Covey008482473manufacture(0096-0709)
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