Label: SAN X E3- 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 January 31, 2022

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  • Active ingredient

    Alcohol 71.0%

  • Purpose

    Hand Sanitizer

  • Uses

    • sanitizes hands to help reduce bacteria that potentially can cause disease
    • helps to prevent cross-contamination
    • recommended for repeated use
    • helps prevent drying of the skin
  • Warnings

    • For external use only
    • Flammable, keep away from fire or flame

    When using this product

    • do not use in or near eyes
    • use in a well-ventilated area

    Stop use and consult a doctor if irritation or redness develop.

    Keep out of reach of children.

    If swallowed, seek medical attention or contact Poison Control Center immediately.

  • Directions

    • wet hands thoroughly with spray, covering entire surfaces of hands, especially the fingernails and cuticles
    • rub hands together until dry
  • Other information

    store in a cool, dry place below 104 F (40 C)

  • Inactive ingredients

    Water, isopropanol, glycerin, glycerol monolaurate

  • Questions?

    Contact Best Sanitizers at 888-225-3267 Mon-Fri 9 am - 4 pm PST

  • PRINCIPAL DISPLAY PANEL

    SAN X

    E3

    Hand

    Sanitizer

    Spray

    • Fragrance and Dye free
    • Kills 99.999% of tested

    pathogens in 15 seconds

    • Meets all FDA (GRAS) and USDA

    requirements for food handling

    • Kosher, Pareve and Halal certified

    NSF

    Nonfood Compounds

    Program Listed E3

    Registration #

    AMERISAN

    Net Contents: 1000mL (33.81 fl. oz)

    container label

  • INGREDIENTS AND APPEARANCE
    SAN X E3 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69884-700
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL LAURATE (UNII: Y98611C087)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69884-700-051000 mL in 1 BOTTLE; Type 0: Not a Combination Product01/31/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/31/2022
    Labeler - Amerisan, LLC (170260090)
    Establishment
    NameAddressID/FEIBusiness Operations
    Best Sanitizers627278224manufacture(69884-700)
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