Label: ARRID XX ROLL ON ANTIPERSPIRANT DEODORANT REGULAR- aluminum chlorohydrate liquid

  • 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 December 15, 2015

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  • Active ingredient

    Aluminum Chlorohydrate (16%)

  • Purpose

    Antiperspirant

  • Use

    reduces underarm perspiration

  • Warnings For external use only

    Do not use on broken skin

    Stop use if rash or irritation occurs

    Ask a doctor before use if you have kidney disease

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Shake gently. Apply a thin layer to underarms only.

  • Inactive ingredients

    Water, Steareth-2, Steareth-21,Dimethicone, Allantoin, Fragrance.

  • Principal Display

    ARRID
    EXTRA EXTRA DRY

    XX

    REGULAR

    ROLL-ON

    Antiperspirant
    Deodorant

    MAXIMUM
    STRENGTH
    PROTECTION

    NET WT. 2.5 FL. OZ. (74mL)

    ARLBF-05062-10

  • INGREDIENTS AND APPEARANCE
    ARRID XX ROLL ON  ANTIPERSPIRANT DEODORANT REGULAR
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62864-901
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE16   in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    STEARETH-2 (UNII: V56DFE46J5)  
    STEARETH-21 (UNII: 53J3F32P58)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62864-901-2574 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35007/16/1996
    Labeler - .Church & Dwight Canada Corp (253933600)
    Registrant - Church & Dwight Co., Inc (001211952)
    Establishment
    NameAddressID/FEIBusiness Operations
    Church & Dwight Canada Corp253933600manufacture(62864-901)
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