Label: BEE SAFE HAND SANITIZER WITH MANUKA HONEY AND LEMONGRASS- 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 July 14, 2021

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

  • Drug Facts

  • Active Ingredient

    Alcohol Denat. 65%

    Purpose

    Antiseptic

  • Use

    Decrease Bacteria on hands

  • Warnings

    Flammable. Keep away from flame or high heat.

    For external use only.

    When using this product

    keep out of eyes.

    Stop use and ask a doctor 

    if irritation or redness develops.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    Rub a dime sized drop into hands.

  • Inactive Ingredients

    Water, Glycerin, Betaine, Triethanolamine, Acrylates/C10-300 Alkyl Acrylate Crosspolymer, Leptospermum Scoparium (Manuka) Mel, Citris Limon Peel Oil, Limonene, Citral.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    BEE SAFE HAND SANITIZER WITH MANUKA HONEY AND LEMONGRASS 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78788-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.65 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BETAINE (UNII: 3SCV180C9W)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    MANUKA OIL (UNII: M6QU9ZUH2X)  
    LEMON OIL (UNII: I9GRO824LL)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    CITRAL (UNII: T7EU0O9VPP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78788-004-308 in 1 CARTON05/01/2020
    130 mL in 1 BOX; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/01/2020
    Labeler - HONEYBUNCH PURE NATURALS NZ LIMITED (671528273)