Label: BLUE SANDALWOOD- hand sanitizer 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 August 6, 2021

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  • Active Ingredient

    Ethyl Alcohol 70% v/v

    Purpose

    Antiseptic

  • Uses

    • To decrease bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only

    Flammable, keep away from fire or flame

    Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin

    Stop use and ask a doctor

    • if irritation and redness develop
    • Condition persists for more than 72 hours

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

  • Directions

    Place enough product in your palm to thoroughly cover your hands

    Children under 6 years of age should be supervised when using this product

    Rub hands together briskly until dry

  • Other Information

    Protect the product in this container from excessive heat and direct sun

    Store below 104F (40C)

    May discolor certain fabrics

  • Inactive Ingredients

    Water, Aloe Barbadensis Leaf Juice, Leuconostoc/Radish Root Ferment Lysate Filtrate, Glycereth-26, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Fragrance, blue 1

  • pouch label

    pouch

  • back label

    back

  • INGREDIENTS AND APPEARANCE
    BLUE SANDALWOOD 
    hand sanitizer spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76150-273
    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
    GLYCERETH-26 (UNII: NNE56F2N14)  
    LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
    LEMON OIL (UNII: I9GRO824LL)  
    LIME OIL (UNII: UZH29XGA8G)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76150-273-5130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/01/2021
    Labeler - Bell International Laboratories, Inc (967781555)
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