Label: HAND SANITIZER FOREST SCENT- ethyl alcohol 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 March 27, 2020

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  • Active lngredient  

    ETHYL ALCOHOL

  • Purpose 

    Antiseptic 

  • Uses

    Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

    Recomended for repeated use.

  • Warnings  

    • For external use only
    • Flammable
    • Keep away from heat and flame.
    •  Do not use in ear , mouth OR eyes.
    • When using this product

      Avoid contact with eyes. In case of eye contact, flush with water.

    • Keep out of reachof children.

    If swallowed, seek medical attention immidately.

  • Directions

    Pump as needed in to your palms and throughly spread on both hand.

    Rub into skin until dry.

  • Inactives 

    Deionized Water, 
    D-Panthenol
    Fragrance
    o-Cymen-5-ol
    Thymus Vulgaris (Thyme) Flower/Leaf Extract

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Product Label  

    product-label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER FOREST SCENT 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73861-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL750 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    O-CYMEN-5-OL (UNII: H41B6Q1I9L)  
    WATER (UNII: 059QF0KO0R)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    THYME (UNII: CW657OBU4N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73861-001-01145 mL in 1 BOTTLE; Type 0: Not a Combination Product03/27/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/23/2020
    Labeler - GREAT EAGLE GROUP INC (113720956)
    Registrant - GREAT EAGLE GROUP INC (113720956)
    Establishment
    NameAddressID/FEIBusiness Operations
    NICE ENTERPRISE CO LTD656089836manufacture(73861-001)
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