Label: ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate spray

  • NDC Code(s): 10565-067-02, 10565-067-04
  • 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, 13% - 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

    Hold two inches from underarm and spray. Use daily for best results.

  • Inactive ingredients

    Purified Water, Isopropyl Alcohol, Propylene Glycol, Peg-40 Hydrogenated Castor Oil, Fragrance.

  • SPL UNCLASSIFIED SECTION

    MFG BY:
    HYDROX LABORATORIES
    825 Tollgate Rd. • Elgin, IL 60123

  • PRINCIPAL DISPLAY PANEL

    Personal Care

    FreshMoment

    Anti-Perspirant
    Deodorant Spray

    Helps Reduce Wetness
    Spring Fresh Fragrance

    MADE IN USA

    2 FL. OZ. (59mL) Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    ANTI-PERSPIRANT DEODORANT 
    aluminum chlorohydrate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10565-067
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10565-067-0259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/11/2011
    2NDC:10565-067-04118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/11/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01911/11/2011
    Labeler - Hydrox Laboratories (025164302)
    Registrant - Hydrox Laboratories (025164302)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hydrox Laboratories025164302manufacture(10565-067) , label(10565-067) , pack(10565-067)
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