Label: HAND SANITIZER LAVENDER- ethyl alcohol spray

  • NDC Code(s): 42681-0006-1
  • Packager: Whole Foods Market, Inc.
  • 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 March 22, 2021

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active ingredient Purpose

    Ethyl Alcohol 62% Antiseptic

  • PURPOSE

    Uses ■ to help reduce bacteria on the skin.

  • WARNINGS

    For external use only. Flammable. Keep away from fire or flame.

  • WHEN USING

    When using this product avoid contact with eyes. If eye contact occurs, rinse with water.

  • STOP USE

    Stop use and ask a doctor if skin irritation or redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    Directions ■ apply 1 to 2 sprays on hands and rub together until dry

  • INDICATIONS & USAGE

  • STORAGE AND HANDLING

    Other information ■ do not store above 104°F (40°C).

  • INACTIVE INGREDIENT

    Inactive ingredients water, isopropyl alcohol, glycerin, fragrance (natural)*, helianthus annuus (sunflower) seed oil, rosmarinus
    officinalis (rosemary) leaf extract, polysorbate 20.

    *Complies within ISO 9235, see www.wholefoodsmarket.com for more information

  • QUESTIONS

    Questions, Comments? ■ customer.questions@wholefoods.com ■ 1-844-936-8255

  • PRINCIPAL DISPLAY PANEL

    Lavender Spray

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  LAVENDER
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42681-0006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ROSEMARY (UNII: IJ67X351P9)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42681-0006-159 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/202012/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/202012/31/2024
    Labeler - Whole Foods Market, Inc. (196175616)
    Registrant - V Manufacturing & Logistics, Inc. (825176857)