Label: PHYSICIANS GROUP HAND SANITIZER GEL- alcohol gel

  • NDC Code(s): 77808-002-01, 77808-002-02, 77808-002-03, 77808-002-04, view more
    77808-002-05
  • Packager: Physicians Group LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2023

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  • Drug Facts

  • Active Ingredient(s)

    Ethyl Alcohol 70% v/v

    Purpose

    Antiseptic

  • Use(s)

    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:

    • on children less than 2 months of age
    • on open skin wounds

    When using this product 

    keep out of eyes, ear 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 contact a Poison Control Center right away.

  • Directions

    • Place enough produt on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other Information

    • Store between 15-30 °C (59-86 °F).
    • Avoid freezing and excessive heat above 40 °C (104° F).
  • Inactive Ingredients

    Purified Water, Glycerin, H.Ethylcellulose, Trienthanolamine, Hydrogen Peroxide

  • Package Labeling:59ml

    Label

  • Package Labeling:120ml

    Label2

  • Package Labeling:237ml

    Label3

  • Package Labeling:473ml

    Label4

  • Package Labeling:3.785L

    Label5

  • INGREDIENTS AND APPEARANCE
    PHYSICIANS GROUP HAND SANITIZER GEL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77808-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77808-002-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product07/14/2020
    2NDC:77808-002-02120 mL in 1 BOTTLE; Type 0: Not a Combination Product07/14/2020
    3NDC:77808-002-03237 mL in 1 BOTTLE; Type 0: Not a Combination Product07/14/2020
    4NDC:77808-002-04473 mL in 1 BOTTLE; Type 0: Not a Combination Product07/14/2020
    5NDC:77808-002-053785 mL in 1 BOTTLE; Type 0: Not a Combination Product07/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/14/2020
    Labeler - Physicians Group LLC (010783019)
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