Label: PHARMACYS PRESCRIPTION 8OZ HAND SANITIZER- alcohol gel

  • NDC Code(s): 72197-011-08
  • Packager: American Consumer Products Corp
  • 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 May 1, 2019

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  • Active Ingredient

    Active Ingredients: Ethyl Alcohol 62%

  • Purpose

    Purpose: Antiseptic

    Uses - Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

  • Warnings

    Warnings - For external use only. Do not swallow.

    Flammable. Keep away from fire or flame.

    Do not apply around eyes. Do not use in ears & mouth.

  • Stop Use

    Stop use and ask a doctor if: If redness or irritation develops and persists for more than 72 hours.

  • Keep out of reach of children

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

  • Inactive Ingredients

    Inactive ingredients - water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, aloe barbadensis gel, carbomer, fragrance.

  • Directions

    Directions - pump as needed into your palms and thoroughly spread on both hands.- rub into skin until dry.

  • Indications & Usage Section

    When using this product, avoid contact with eyes. In case of contact, flush eyes with water.

  • Other Information

    Other Information - store at 20o C (68o to 77o F).

    - may discolor fabrics.

  • Pharmacy's Prescription 8 OZ Label

    Pharmacy's Prescription 8 OZ Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    PHARMACYS PRESCRIPTION 8OZ HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72197-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TRIETHANOLAMINE 2-CYCLOHEXYL-4,6-DINITROPHENOLATE (UNII: N2TK31JIAH)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    ALOE ARBORESCENS WHOLE (UNII: 0EF00WD7LU)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL 2-(2-METHYLBUTYRATE) (UNII: 3Z73C506A9)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72197-011-08237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/01/2019
    Labeler - American Consumer Products Corp (081101181)
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