Label: ANTI-PERSPIRANT DEODORANT ROLL-ON UNSCENTED- aluminum chlorohydrate liquid

  • NDC Code(s): 10565-074-01, 10565-074-02
  • Packager: Hydrox Laboratories
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 26, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum Chlorohydrate, 10% - Anhydrous Basis

  • Purpose

    Antiperspirant

  • Use

    Reduces underarm wetness.

  • Warnings

    FOR EXTERNAL USE ONLY.

    KEEP OUT OF REACH OF CHILDREN.

    Do not use on broken skin.

    Stop use if rash or irritation occurs.

    Ask a doctor before use if you havekidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

  • Directions

    Apply to underarms. Use daily for best results.

  • Inactive ingredients

    Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Tetrasodium EDTA

  • PRINCIPAL DISPLAY PANEL 

    Personal Care

    FreshMoment

    Anti-Perspirant

    Deocorant Roll-On

    Alcohol Free

    Helps Reduce Wetness

    Fragrance Free

    Dye Free Formula

    Made in USA

    PRINCIPAL DISPLAY PANEL

  • INGREDIENTS AND APPEARANCE
    ANTI-PERSPIRANT DEODORANT ROLL-ON  UNSCENTED
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10565-074
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE10 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10565-074-0145 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/20/2012
    2NDC:10565-074-0259 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/20/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01903/20/2012
    Labeler - Hydrox Laboratories (025164302)
    Registrant - Hydrox Laboratories (025164302)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hydrox Laboratories025164302label(10565-074) , manufacture(10565-074) , pack(10565-074)
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