Label: ORGANIC LAVENDER HAND SANITIZER- alcohol gel 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 March 24, 2016

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

  • Active Ingredients

    Active Ingredients

    Organic SD Alcohol 60

    Purpose

    Antimicrobial

  • Directions

    Spray into palms, rub hands together until dry. Repeat as needed.

  • Warnings

  • Drug Facts

    Organic SD Alcohol 60%

  • Purpose

    Antimicrobial

  • Warnings

    Keep out of reach of children

  • Inactive Organic Ingredients

    Aloe Barbadensis Juice, Glycerin, Cocos Nucifera (Coconut) Oil, Lavandula Angustifolia Oil, Ocimum Basillicum (Basil) Extract, Cinnamomum Cassia Bark Extract, Cymbopogon Schoenanthus (Lemongrass) Oil

  • Aroma Bella Organic Lavender Hand Sanitizer 12mL

    Aroma Bella
    Organic Lavender Hand Sanitizer 12mL

    Lavender Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    ORGANIC LAVENDER HAND SANITIZER 
    alcohol gel liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69580-060
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)  
    BASIL OIL (UNII: Z129UMU8LE)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69580-060-0112 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/16/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/30/2015
    Labeler - Royal Labs Natural Cosmetics, Inc (197478480)