Label: HAND SANITIZER- 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 August 19, 2020

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  • Active Ingredient(s)

    Alcohol 65% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only, Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge

  • Do not use

    • In eyes | on children less than 2 months of age | on open skin wounds
  • When using this product

    If in eyes, rinse promptly and thoroughly with water | Discontinue use if irritation and redness develops

  • Stop use and ask a doctor

    If skin irritation or redness occurs or persists for more than 72 hours.

  • Keep out of reach of children.

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

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    For additional information, see Safety Data
    Sheets (SDS) | For emergency medical information in USA and
    Canada, call 1-888-255-3924 | Store between 15-
    30C (59-86F) | Avoid freexing and excessive heat above 40C
    (104F)

  • Inactive ingredients

    water (aqua), propylene glycol,
    dimethicone PEG-7 Isostearate, acrylates/ C10-30 Alkyl
    Acrylate Crosspolymer, aminomethylpropanediol, tocopherol
    acetate, aloe barbadensis leaf juice

  • Package Label - Principal Display Panel

    59 mL NDC: 79436-102-0159 mL NDC: 79436-102-01

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79436-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79436-102-0140000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/19/2020
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/19/2020
    Labeler - Oingo Products LLC (117510957)
    Registrant - Oingo Products LLC (117510957)
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