Label: ADVENTURE HAND SANITIZER - FRAGRANCE 80%- alcohol spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 20, 2022

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  • Active ingredient

    Ethyl Alcohol 80% v/v

  • Purpose

    Antimicrobial

  • Use

    For hand sanitizing to decrease bacteria on skin.

  • Warnings

    For external use only

    Flammable, keep away from fire and flame

    Do not use

    in the eyes

    Keep out of reach of children

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

    Stop use and ask a doctor if

    redness or irritation develops and persists for more than 72 hours

  • Directions

    Spray hands thoroughly. Rub hands together until dry.

  • Inactive ingredients

    Water, Propanediol, Aloe Vera Powder, Panthenol, Hydroxyethylcellulose

  • Label

    Adventure Hand Santitizer

    By the makers of Shower Pouch

    Remove odors

    Kills germs on the go

    1.3 fl oz [38 ml]

    front

    Back

  • INGREDIENTS AND APPEARANCE
    ADVENTURE HAND SANITIZER - FRAGRANCE 80% 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77371-124
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.8 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77371-124-0138 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/05/2020
    Labeler - NICETY SOLUTIONS LLC (030405122)
    Registrant - NICETY SOLUTIONS LLC (030405122)
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