Label: LUCKY INSTANT HAND SANITIZER CITRUS ZEST- ethyl alcohol 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 September 30, 2019

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  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    Hand Sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

  • Warnings

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



  • When using this product

    avoid contact with the skin and mucous membranes. I case of eye contact, immediately flush eyes with water, call a doctor. Avoid contact with broken skin.

    Discontinue use if irritation develops. If condition persists for more than 72 hours, consult a doctor.

  • Keep out of reach of children

    Children can only use this product with adult supervision. Do not drink. Not edible. In case of accidental ingestion seek professional assistance or Poison Control Center immediately.

  • Other information

    Do not store above 105ºF. May discolor some fabrics. Harmful to wood finishes and plastics.

  • Directions

    Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Recommended for repeated use.

  • INACTIVE INGREDIENT

    Deionized Water, Isopropyl Alcohol, Glycerin, Carbomer, Triethanolamine, Propylene Glycol, PEG-40 Hydrogenated Castor Oil, Fragrance, Alphatocopherol Acetate (Vitamin E), FDC Yellow 5

  • Package Label


    image of package label

  • INGREDIENTS AND APPEARANCE
    LUCKY INSTANT HAND SANITIZER CITRUS ZEST 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-156
    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)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:20276-156-6060 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2010
    2NDC:20276-156-022 in 1 BLISTER PACK03/01/2010
    2NDC:20276-156-6060 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    3NDC:20276-156-05148 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2010
    4NDC:20276-156-08237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2010
    5NDC:20276-156-10296 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2010
    6NDC:20276-156-12355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2010
    7NDC:20276-156-24710 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2010
    8NDC:20276-156-361065 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2010
    9NDC:20276-156-401183 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2010
    10NDC:20276-156-481420 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2010
    11NDC:20276-156-641893 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2010
    12NDC:20276-156-853785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/01/2010
    Labeler - Delta Brands Inc (102672008)
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