Label: 2.5OZ EVERDRY ANTIPERSPIRANT INVISIBLE- aluminum chlorohydrate gel stick

  • NDC Code(s): 72197-017-02
  • Packager: American Consumer Products Corp
  • Category: HUMAN OTC DRUG LABEL

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 May 17, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredients: Aluminum Chlorohydrate 20%

  • PURPOSE

    Purpose: Antiperspirant

  • WARNINGS

    Warnings: For external use only.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.

  • INACTIVE INGREDIENT

    Ingredients: Mineral Oil, Stearic Acid, Stearyl Alcohol, Zinc Palmitate, Cyclopentasiloxane, Hydrogenated Castor Oil, Fragrance, Silica, PPG-14 Butyl Ether, PEG-8 Disterate, BHT.

  • DOSAGE & ADMINISTRATION

    Directions: Twist base. Smooth onto dry underarms. Apply to underarms only.

  • INSTRUCTIONS FOR USE

    Use: reduces underarm wetness and perspiration.

  • STOP USE

    Stop use and ask a doctor if irritation or rash develops.

  • INDICATIONS & USAGE

    Do not use on broken or irritated skin.

  • PRINCIPAL DISPLAY PANEL

    EverDry Anti Perspirant

  • INGREDIENTS AND APPEARANCE
    2.5OZ EVERDRY ANTIPERSPIRANT INVISIBLE 
    aluminum chlorohydrate gel stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72197-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ZINC PALMITATE (UNII: Q7407964JA)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    PEG-8 DISTEARATE (UNII: 7JNC8VN07M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72197-017-0264 g in 1 TUBE; Type 0: Not a Combination Product09/17/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35009/17/2019
    Labeler - American Consumer Products Corp (081101181)
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!