Label: BABARIA DOUBLE EFFECT DEODORANT AND ANTIPERSPIRANT LIQUID ROLL-ON- aluminum chlorohydrate emulsion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 20, 2023

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  • Drug Facts

  • Active ingredient

    Aluminum chlorohydrate 20%

    Purpose

    Antiperspirant

  • Uses

    • Reduces underarm sweat
    • 24 hour effective protection
  • 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 Posion Control Center right away.

  • Directions

    Apply to underarms only

  • Inactive ingredients

    Water (aqua), steareth-2, glycerin, steareth-21, tocopherol acetate octenidine HCL, creosote bush (Larrea tridentata var, tridentata) extract, tocopherol, dimethicone fragrance (parfum), biotin, lecithin, phenoxyethanol, sodium hydroxide, propylene glycol, ethylhexylglycerin, dehydroacetic acid, benzoic acid, sorbic acid, butylene glycol, ascorbic acid, sodium citrate, potassium sorbate, citric acid, sodium metabisulfite, limonene, linalool, hexyl cinnamal.

  • Package Labeling:

    Bottle2

  • INGREDIENTS AND APPEARANCE
    BABARIA DOUBLE EFFECT DEODORANT AND ANTIPERSPIRANT LIQUID ROLL-ON 
    aluminum chlorohydrate emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78283-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE200 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LARREA TRIDENTATA WHOLE (UNII: B755J144H1)  
    WATER (UNII: 059QF0KO0R)  
    STEARETH-2 (UNII: V56DFE46J5)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEARETH-21 (UNII: 53J3F32P58)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    BIOTIN (UNII: 6SO6U10H04)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    SORBIC ACID (UNII: X045WJ989B)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78283-003-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product03/18/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01903/18/2024
    Labeler - BERIOSKA SL (462392556)
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