Label: HAND SANITIZER gel

  • NDC Code(s): 41366-052-01
  • Packager: Zhejiang Meimi Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 20, 2024

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  • Active Ingredient(s)

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Use

    Uses hand sanitizer to help reduce bacteria on skin.

  • Warnings

    • For external use only.
    • Flammable. Keep away from heat or flame.
  • Do not use

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

  • STOP USE

    Stop use and ask a doctor if irritation, excessive redness or rash develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. Supervise children under 6 years of age when using this product to avoid swallowing. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Put a dime sized drop onto hands and rub together briskly until dry.

  • Other information

    Store below 110℉(43℃).

  • Inactive ingredients

    Water, glycerin, propylene glycol, fragrance, carbomer, triethanolamine, red 33, blue 1.

  • Package Label - Principal Display Panel

    59 mL in 1 BOTTLE NDC: 41366-052-01

    59ml label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41366-052
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    BERBERIS ARISTATA FRUIT (UNII: U612N9372B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41366-052-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product04/18/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/18/2022
    Labeler - Zhejiang Meimi Technology Co., Ltd. (413668440)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Meimi Technology Co., Ltd.413668440manufacture(41366-052)
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