Label: VENTURE ANTIPERSPIRANT DEODORANT (FRAGRANCE)- aluminum chlorohydrate spray

  • 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 July 14, 2022

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  • Active ingredient

    Aluminum Chlorohydrate 18%

  • Purpose

    Antiperspirant

  • Use

    For underarm use to decrease wetness.

  • Warnings

    For external use only

    Flammable, keep away from fire and flame

    Do not use

    on broken skin

    Ask a doctor before use if you have

    kidney disease

    Stop use

    if rash or irritation occurs

    Keep out of reach of children

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

  • Directions

    Shake before use. Apply to underarms only.

  • Inactive ingredients

    Water, Ethanol, Glycerin, Panthenol, Propanediol, Aloe Vera, Ceteareth-25, PEG-8 Dimethicone, Fragrance

  • Label

    Venture Deodorant

    By the makers of Shower Pouch

    Fragrance

    Antiperspirant, Sharable, Vegan

    1.3 fl oz [38.5 ml]

    Label

  • INGREDIENTS AND APPEARANCE
    VENTURE ANTIPERSPIRANT DEODORANT (FRAGRANCE) 
    aluminum chlorohydrate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77371-131
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE15 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    CETEARETH-25 (UNII: 8FA93U5T67)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77371-131-0138 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM01907/01/2022
    Labeler - NICETY SOLUTIONS LLC (030405122)
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