Label: COOL FOOT- antiperspirant spray

  • 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 September 3, 2013

If you are a consumer or patient please visit this version.

View All Sections
  • PRINCIPAL DISPLAY PANEL

    box image

  • ACTIVE INGREDIENT

    Active Ingredients

    Aluminum Chlorohydrate 15.0%

  • PURPOSE

    Uses

    Treats excessive perspiration

    Reduses wetness

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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

  • INDICATIONS & USAGE

    Foot Spray With Odor Control

  • WARNINGS

    Warnings For external use only

    Do not use On broken skin On an area that is infected or reddened

    When using this product Do not use in or near eyes apply to sole and foot area only

    Stop use an ask a doctor if rash, irritation or sensitivity develops

    Ask a doctor before use if you have kidney disease

  • DOSAGE & ADMINISTRATION

    Directions

    This product should be sprayed on the feet, Product can be applied daily morning and night

  • INACTIVE INGREDIENT

    Inactive Ingredients: Ethanol, Water, PPG-15 Stearyl Ether, PPG-5-Ceteth-20, Oleth-10, Menthol, Parfum

  • INGREDIENTS AND APPEARANCE
    COOL FOOT 
    antiperspirant spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59305-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE12 g  in 125 g
    Inactive Ingredients
    Ingredient NameStrength
    ACETALDEHYDE (UNII: GO1N1ZPR3B)  
    water (UNII: 059QF0KO0R)  
    PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
    PPG-5-CETETH-20 (UNII: 4AAN25P8P4)  
    OLETH-10 (UNII: JD797EF70J)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59305-030-01125 g in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35007/10/2013
    Labeler - NEAT FEAT PRODUCTS (199291597)
    Establishment
    NameAddressID/FEIBusiness Operations
    NEAT FEAT PRODUCTS199291597manufacture(59305-030)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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