Label: CERTAIN DRI- aluminum chlorohydrate cloth

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

Drug Label Information

Updated December 23, 2025

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

  • ACTIVE INGREDIENT

  • PURPOSE

    Active ingredient (in each wipe)Purpose
    Aluminum chlorohydrate 15%Antiperspirant
  • INDICATIONS & USAGE

    Usereduces underarm perspiration

  • Warnings

    For external use only

  • DO NOT USE

    Do not use

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

    Ask a doctor before use ifyou have kidney disease

  • WHEN USING

    When using this product

    • do not use in or near eyes
    • apply to underarms only
  • KEEP OUT OF REACH OF CHILDREN

  • 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

    • open packet
    • remove and unfold wipe
    • apply to underarm only
  • Inactive ingredients

    benzoic acid, benzyl alcohol, chlorphenesin, fragrance, PEG-180, phenoxyethanol, polysorbate 20, potassium sorbate, salvia offcinalis (sage) leaf extract, sorbic acid, tocopherol, tocopheryl acetate, usnea barbata (lichen) extract, water

  • QUESTIONS

    Questions? c all 1-844-923-7837

  • PRINCIPAL DISPLAY PANEL

    CERTAIN
    DRI ®

    CLINICAL STRENGTH

    ALUMINUM CHLOROHYDRATE 15%

    1 ANTIPERSPIRANT WIPE

    SKIN-FRIENDLY INGREDIENTS | DRIES QUICKLY | NO RESIDUE OR STICKINESS

    Distributed by: Certain Dri LLC
    811 Broad Street, Suite 600
    Chattanooga, TN 37402 ©2023

    1000166

    CRUELTY
    FREE

    Packet Label
  • INGREDIENTS AND APPEARANCE
    CERTAIN DRI 
    aluminum chlorohydrate cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69693-725
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE0.15 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SALVIA OFFICINALIS FLOWERING TOP (UNII: 48JCS720FN)  
    SORBIC ACID (UNII: X045WJ989B)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    USNEA BARBATA (UNII: D6DVA9TCAP)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (TOWLETTE PRE-MOISTENED WITH ANTIPERSPIRANT LIQUID) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69693-725-0630 g in 1 PACKET; Type 0: Not a Combination Product10/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01910/01/2023
    Labeler - Clarion Brands, LLC (079742703)