Label: PURCOL MOISTURIZING HAND SANITIZER- 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 March 1, 2022

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  • Drug Facts

  • Active Ingredient

    Ethyl alcohol 70% v/v

    Purpose

    Antimicrobial

  • Uses

    • Hand sanitizer to help reduce bacteria on the skin that could cause disease
    • Recommended for repeated use
  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only

    When using this product

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

    Stop use and ask a doctor if

    irritation or rash appears and lasts.   

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product in your palm to thoroughly cover your hands
    • Rub hands together until dry
    • No rinsing required
    • No towels needed
  • Other Information

    • Store below 104°F (40°C)
    • May discolor certain fabrics or surfaces
  • Inactive Ingredients

    Water, Glycerin, Aloe Barbadensis Leaf Extract, Hydroxypropyl cellulose, Lauryl lactate, Myristyl lactate, Cetyl lactate, Fragrance.

  • Package Labeling:60ml

    Label

  • Package Labeling:251.3ml

    Label2

  • Package Labeling:473.1ml

    Label3

  • INGREDIENTS AND APPEARANCE
    PURCOL MOISTURIZING HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75266-685
    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)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    LAURYL LACTATE (UNII: G5SU0BFK7O)  
    MYRISTYL LACTATE (UNII: 1D822OC34X)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75266-685-6060 mL in 1 TUBE; Type 0: Not a Combination Product04/29/2020
    2NDC:75266-685-61251.3 mL in 1 BOTTLE; Type 0: Not a Combination Product04/29/2020
    3NDC:75266-685-62473.1 mL in 1 BOTTLE; Type 0: Not a Combination Product04/29/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/29/2020
    Labeler - Purocol LLC (117479056)
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