Label: 75% ALCOHOL HAND SANITIZER- hand sanitizer solution

  • 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 7, 2020

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  • Active Ingredient(s)

    Alcohol 75% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    For hand-washing to decrease bacteria on the skin.

  • Warnings

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

  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.



    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.



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

  • Do not use

    Stop use and ask doctor if irritation and redness develop.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or call Poison Control Center right away.

  • Directions

    • Deposit a dime size amount of product onto palm of hand.
    • Rub hands together until dry.
  • Inactive ingredients

    Aminomethylpropanol, carbopol 980 polymer, glycerin, propylene glycol, sterile distilled water.

  • Package Label - Principal Display Panel

    30mL NDC: 72922-014-01 Package LabelPackage Label

  • Package Label - Principal Display Panel

    60 mL NDC: 72922-014-02 Package LabelPackage Label

  • Package Label - Principal Display Panel

    ​29 mL NDC: 72922-014-03 Package LabelPackage Label

  • INGREDIENTS AND APPEARANCE
    75% ALCOHOL HAND SANITIZER 
    hand sanitizer solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72922-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.5 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 100 mL
    CARBOMER 980 (UNII: 4Q93RCW27E) 0.3 mL  in 100 mL
    WATER (UNII: 059QF0KO0R) 23.5 mL  in 100 mL
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.2 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72922-014-0130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    2NDC:72922-014-0260 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    3NDC:72922-014-0329 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/01/2020
    Labeler - Shangrao Chunyu Technology Co.,ltd. (541569308)
    Registrant - Shangrao Chunyu Technology Co.,ltd. (541569308)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shangrao Chunyu Technology Co.,ltd.541569308manufacture(72922-014)
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