Label: CERTAIN DRI ANTIPERSPIRANT FOOT-LOTION- aluminum chloride lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 23, 2025

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  • Active ingredient 

    Aluminum chloride 15%

  • Purpose

    Antiperspirant

  • Warnings

    For external use only

  • Do not use

    • on broken or irritated skin
    • immediately after shaving
    • immediately after bathing
  • ASK DOCTOR

    Ask a doctor before use if you havekidney disease

  • WHEN USING

    When using this productdo not use in or near eyes

  • STOP USE

    Stop use and ask a doctor ifrash or irritation develops

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    • wash and dry soles thoroughly before application
    • apply a small, pea sized amount to the soles of your feet
    • rub into soles vigorously for 15 seconds 
    • for best results, apply every night before bed and an additional two times per day for at least four weeks
  • Inactive ingredients

    aloe barbadensis leaf juice, artemisia vulgarixs extract, behentrimonium methosulfate, bisaolol, bis-laurl cocaminopropylamine/HDI/PEG-100 copolymer, butylene glycol, cetearyl alcohol, cetyl alcohol, dimethicone, ethylhexyglycerin, hydroxyethylcellulose, jojoba esters, laminaria digitata extract, opuntia ficus-indica fruit extract, potassium hydroxide, saccharomyces cerevisiae extract, water, zingiber officinale (ginger) root extract

    Questions? call  1-844-923-7837

  •  

  • QUESTIONS

  • PACKAGE LABEL

    CERTAIN
    DRI ®
    ANTIPERSPIRANT

    QUICK DRY
    SWEAT
    GUARD

    FOOT
    LOTION

    CLINICALLY SHOWN
    TO REDUCE SWEAT

    NET WT 1.3 OZ (36 g)

    Distributed by: Certain Dri LLC, 811 Broad Street, Suite 600
    Chattanooga, TN 37402 ©2024

    1000163

    foot lotion label
  • INGREDIENTS AND APPEARANCE
    CERTAIN DRI ANTIPERSPIRANT FOOT-LOTION 
    aluminum chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69693-726
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE0.15 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)  
    BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    THIAMINE BIS-LAURYLSULFATE (UNII: 226A8HU328)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    LAMINARIA DIGITATA (UNII: 15E7C67EE8)  
    OPUNTIA FICUS-INDICA FRUIT JUICE (UNII: 5ZC110ZY2H)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)  
    WATER (UNII: 059QF0KO0R)  
    GINGER (UNII: C5529G5JPQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69693-726-141 in 1 CARTON09/01/2024
    136 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01909/01/2024
    Labeler - Clarion Brands, LLC (079742703)
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