Label: HI AND DRI ANTIPERSPIRANT ROLL-ON POWDER FRESH- aluminum chlorohydrate liquid

  • Category: HUMAN OTC DRUG LABEL

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 9, 2013

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  • Drug Facts Active Ingredient

    Aluminum chlorohydrate 18%

  • Purpose

    Antiperspirant

  • Use

    • Reduces underarm wetness
  • Warnings:

    For external use only.

    Do not use on broken skin

    Ask a doctor before use if you have kidney disease

    Stop use if rash or irriation occurs

  • 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

    aqua((water) eau), glyceryl stearate, laureth-23, magnesium aluminum silicate, laureth-4, lauric acid, cetearyl alcohol, behentrimonium methosulfate, edta, alpha-isomethyl ionone, citronellol, limonene, hydroxycitronellol, benzyl alcohol, benzyl salicylate, linalool, citral

  • Questions

    1-800-473-8566

  • Principal Display Panel - 1.7 fl oz bottle

    MM1

  • INGREDIENTS AND APPEARANCE
    HI AND DRI ANTIPERSPIRANT  ROLL-ON POWDER FRESH
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10967-057
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE0.18 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    LAURETH-23 (UNII: N72LMW566G)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    LAURETH-4 (UNII: 6HQ855798J)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    GERANIOL (UNII: L837108USY)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    LINALOOL, (+)- (UNII: F4VNO44C09)  
    CITRAL (UNII: T7EU0O9VPP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10967-057-9750 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35001/01/1982
    Labeler - Revlon Consumer Products Corp (788820165)
    Establishment
    NameAddressID/FEIBusiness Operations
    Revlon South Africa (PTY) Ltd637155859manufacture(10967-057)
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