Label: OKAY WOMENS ANTIPERSPIRANT ROLL ON DEODORANT- aluminum chlorohydrate liquid

  • NDC Code(s): 74553-009-01
  • Packager: Xtreme Tools International, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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 June 23, 2021

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  • Active Ingredient

    Aluminum Chlorohydrate (15%)…………………………………………..Purpose :Antiperspirant

  • Purpose

    Antiperspirant

  • Uses

    Reduces underarm wetness.

  • Warnings

    For external use only.

  • DO NOT USE

    Do not use on broken skin.

  • STOP USE

    Stop Use and ask doctor if Rash or irritation occurs.

  • ASK DOCTOR

    Ask a doctor before use if you have kidney disease.

  • 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

    Apply to underarms only.

  • Inactive Ingredients

    Deionized Water, Propanediol, Polyglyceryl-10-Caprylate/Caprate, Fragrance.

  • Questions or comments?

    Call 1-305-622-7474 Monday-Friday 9:00 AM to 5:00 PM

  • PACKAGE LABEL

    2 OZ (56 g) Roll on Tube (NDC 74553-009-01)

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  • INGREDIENTS AND APPEARANCE
    OKAY WOMENS ANTIPERSPIRANT ROLL ON DEODORANT 
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74553-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    POLYGLYCERYL-10 CAPRYLATE (UNII: YS396CQX5C)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74553-009-0156 g in 1 TUBE; Type 0: Not a Combination Product06/07/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35006/07/2021
    Labeler - Xtreme Tools International, Inc (125398904)
    Registrant - Xtreme Tools International, Inc (125398904)
    Establishment
    NameAddressID/FEIBusiness Operations
    Xtreme Tools International, Inc125398904manufacture(74553-009)
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