Label: BABARIA OAT FRESH DEODORANT AND ANTIPERSPIRANT LIQUID ROLL-ON- aluminum chlorohydrate emulsion

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

Drug Label Information

Updated December 20, 2023

If you are a consumer or patient please visit this version.

  • 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, oat (avena sativa) kernel extract, octenidine HCL, ethylhexylglycerin, propylene glycol, Polysorbate 80, fragrance (parfum), phenoxyethanol, sodium hydroxide, dehydroacetic acid, benzoic acid, sorbic acid, potassium sorbate, sodium benzoate, D&C Yellow No.10 (CI 47005), FD&C Yellow No.5 (CI 19140), FD&C Red No.40 (CI 16035), benzyl alcohol, citronellol, coumarin, eugenol, hexyl cinnamal, linalool, alpha-isomethyl ionone.

  • Package Labeling:

    Bottle3

  • INGREDIENTS AND APPEARANCE
    BABARIA OAT FRESH DEODORANT AND ANTIPERSPIRANT LIQUID ROLL-ON 
    aluminum chlorohydrate emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78283-005
    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
    WATER (UNII: 059QF0KO0R)  
    STEARETH-2 (UNII: V56DFE46J5)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEARETH-21 (UNII: 53J3F32P58)  
    AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)  
    OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    SORBIC ACID (UNII: X045WJ989B)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    COUMARIN (UNII: A4VZ22K1WT)  
    EUGENOL (UNII: 3T8H1794QW)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78283-005-0150 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)