Label: GREASE MAGIC HAND SANIITIZER- 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 January 26, 2022

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  • Active Ingredient

    Alcohol 80% v/v.

  • Purpose

    Antiseptic

  • Uses

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

  • Warnings

    For external use only. Flammable keep away from heat or flame.

    Do not use if irritation or rash develop. these may be signs of serious condition and persist.

    when using this product do not smoke

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

  • Inactive ingredients

    Glycerin, Hydrogen peroxide, purified water USP

  • SPL UNCLASSIFIED SECTION

    Other information

    store between 15-30C(59-86F). Avoid freezing and excessive heat above 40C.

    Keep away from open flame and heat. to avoid breathing vapors on mist open in well ventilated or outside places. if you experience
    eye watering, headache dizziness, increase fresh air or wear respiratory protection or leave the area.

    PRECAUTIONARY statements: do not smoke while using this product. do not use near open flames or while welding.

    First aid: if swallowed do not induce vomiting do seek physician immediately in case of eye contact thoroughly wash eyes for up 10 15 minutes and seek a physician immediately.
    notice: reports have associated repeated and prolonged occupational over exposure to certain solvents can be harmful possibly fatal.

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    GREASE MAGIC HAND SANIITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:90064-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:90064-001-01236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2020
    2NDC:90064-001-02473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2020
    3NDC:90064-001-03946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2020
    4NDC:90064-001-043785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2020
    5NDC:90064-001-05208198 mL in 1 DRUM; Type 0: Not a Combination Product08/12/2020
    6NDC:90064-001-061040990 mL in 1 CONTAINER; Type 0: Not a Combination Product08/12/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/12/2020
    Labeler - NU-TECH CLEANING SYSTEMS, INC. (825717622)