Label: BESAFE- alcohol liquid

  • 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 November 14, 2022

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  • Active Ingredient

    Alcohol 70% v/v.

  • Purpose

    Antiseptic

  • Use

    To decrease bacteria on the skin that could cause disease. recommended for repeated use

  • Warnings

    For external use only: hands
    Flamable, keep away from fire or flame
    When using this product Keep out of eyes.In case of contact with eyes, flush throughly with water. Avoid contact with broken skin. Do not inhale or ingest

    Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours

    Other information

    Do not store above 105°F may discolor some fabrics. harmful to wood finishes and plastics

  • Keep out of reach of children

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

  • Directions

    Spray hands throughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants

  • Inactive ingredients

    Water, Glycerin, Aloe barbadensis leaf juice, Tocopheryl acetate, Fragrance 

  • Package Label - Principal Display Panel

    59 mL Label

    59 mL Label

  • INGREDIENTS AND APPEARANCE
    BESAFE 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72283-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72283-020-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/15/2020
    Labeler - Alternative Laboratories LLC (029418137)
    Establishment
    NameAddressID/FEIBusiness Operations
    Alternative Laboratories LLC029418137manufacture(72283-020)
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