Label: MICROBE BLOC HAND SANITIZER- benzalkonium chloride lotion

  • 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 4, 2021

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  • SPL UNCLASSIFIED SECTION

    DRUG FACTS

  • Active Ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antiseptic

  • Uses

    Hand sanitizing and to decrease bacteria on the skin.

  • Warnings

    For external use only.

    Do not use in the eyes.

    In case of eye contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor

    if irritation or redness develops, or if condition persists more than 72 hours.

    Keep out of reach of children.

    Instruct children on proper use. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Apply a small amount to hands and rub until dry. Lotion does not replace soap and water.

  • Inactive Ingredients

    Aloe Barbadensis Extract, Avena Sativa (Oat) Extract, Behentrimonium Methosulfate, Caprylyl Glycol, Cetearyl Alcohol, Cetrimonium Chloride, Dimethicone, Glycerin, Hydrolyzed Soy Protein, Mentha Piperita (Peppermint) Essential Oil, Phenoxyethanol, Polysorbate 60, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Vitamin A Palmitate, Vitamin E Acetate, Water.

  • PRINCIPAL DISPLAY PANEL

    MICROBE

    BLOC
    HAND SANITIZER LOTION
    ALCOHOL-FREE
    2 fl. oz. (59mL)

    www.preferredplusmedical.com

    MICROBE BLOC HAND SANITIZER LOTION ALCOHOL-FREE 2 fl. oz. (59mL) www.preferredplusmedical.com

  • INGREDIENTS AND APPEARANCE
    MICROBE BLOC HAND SANITIZER 
    benzalkonium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69243-1112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0013 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AVENA SATIVA LEAF (UNII: 206PI19V7R)  
    BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SOY PROTEIN (UNII: R44IWB3RN5)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    JOJOBA OIL (UNII: 724GKU717M)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69243-1112-144 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2021
    2NDC:69243-1112-259 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2021
    3NDC:69243-1112-3118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2021
    4NDC:69243-1112-4237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2021
    5NDC:69243-1112-5473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2021
    6NDC:69243-1112-6946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2021
    7NDC:69243-1112-73785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333A03/01/2021
    Labeler - Willspeed Technologies LLC (019063540)
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