Label: LACTOVIT SENSITIVE SKIN ROLL-ON ANTIPERSPIRANT DEODORANT- 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 16, 2009

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  • ACTIVE INGREDIENT

    Active Ingredient

    Aluminum Chlorohydrate 10 percent

  • PURPOSE

    Purpose

    Antiperspirant

  • INDICATIONS & USAGE

    Uses

    - Reduces underarm wetness.

  • DOSAGE & ADMINISTRATION

    Directions

    - Apply to underarms only.

  • WARNINGS

    - For external use only.

    - Do not use on broken skin.

  • STOP USE

    - Stop use if rash or irritation occurs.

  • ASK DOCTOR

    - Ask a doctor before using if you have kidney disease.

  • KEEP OUT OF REACH OF CHILDREN

    - Keep out of reach of children. If swallowed, get medical help or
      contact Poison Control Center right away.

  • STORAGE AND HANDLING

    Other Information:

    Store at room temperature.

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Acetyl Dipeptide-3 Amino-hexanoate, Allantoin, Ascorbic Acid, BHT,

    Bisabolol, Butylene Glycol, Cyclopentasiloxane, Edetate Disodium,

    Fragrance, Hydrolyzed Milk Protein, Phenoxyethanol, PPG-15 Stearyl

    Ether, Propyl Gallate, Spirulina Platensis Extract, Steareth-2, Steareth-21,

    Triclosan, Water

  • PRINCIPAL DISPLAY PANEL

    Manufactured by:

    Antonio Puig S.A.

    Travessera de Gracia, 9

    Barcelona E-08021

    Spain

    Made in Spain

  • PRINCIPAL DISPLAY PANEL

    Antonio Puig Lactovit Sensitive Skin Front

  • PRINCIPAL DISPLAY PANEL

    Antonio Puig Lactovit Sensitive Skin Back

  • INGREDIENTS AND APPEARANCE
    LACTOVIT SENSITIVE SKIN ROLL-ON ANTIPERSPIRANT DEODORANT 
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50007-2000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLOROHYDRATE10 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYL GALLATE (UNII: 8D4SNN7V92)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50007-2000-150 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35012/16/2009
    Labeler - Antonio Puig, S.A. (460013279)
    Registrant - Antonio Puig, S.A. (460013279)
    Establishment
    NameAddressID/FEIBusiness Operations
    Antonio Puig, S.A.460013279manufacture
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