Label: LA BODIES PURITA ANTI-BACTERIAL HAND SANITIZER- alcohol gel

  • 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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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients

    Ethyl Alcohol 62%

  • Purpose

    Antimicrobial

  • Inactive Ingredients

    Water (Aqua), Propylene Glycol, Aloe Barbadensis Leaf Juice, Glycerin, Tocopheryl Acetate, Carbomer, Triethanolamine, Fragrance (Parfum)

  • Use

    Hand Sanitizer to help reduce bacteria on the skin

  • Warnings

    • Flammable. Keep away from fire or flame. For external use only.
    • When using this product do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.
    • Stop use and ask doctor if irritation or rash appears and lasts.

    • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
  • Directions

    Place product on hands. Rub until dry.

  • SPL UNCLASSIFIED SECTION

    Manufactured by:
    Samson Pharmaceuticals Inc.
    Commerce, CA 90040

  • PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label

    KILLS 99.99%
    of GERMS

    MADE IN
    U.S.A.

    Purita™

    LA
    Bodies    ™

    Anti-Bacterial
    HAND SANITIZER
    with Moisturizer & Vitamin E

    H1N1 Antiviral

    NET WT 2 FL OZ (59 ml)

    PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label
  • INGREDIENTS AND APPEARANCE
    LA BODIES PURITA ANTI-BACTERIAL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20146-4009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    propylene glycol (UNII: 6DC9Q167V3)  
    aloe vera leaf (UNII: ZY81Z83H0X)  
    glycerin (UNII: PDC6A3C0OX)  
    .alpha.-tocopherol acetate (UNII: 9E8X80D2L0)  
    carbomer homopolymer type c (allyl pentaerythritol crosslinked) (UNII: 4Q93RCW27E)  
    trolamine (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:20146-4009-159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2015
    2NDC:20146-4009-2236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2015
    3NDC:20146-4009-3473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2015
    Labeler - SAMSON PHARMACEUTICAL (088169581)
    Establishment
    NameAddressID/FEIBusiness Operations
    SAMSON PHARMACEUTICAL088169581MANUFACTURE(20146-4009)
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