Label: IDLIFE SANITIZE MOISTURIZING 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 January 14, 2022

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  • SPL UNCLASSIFIED SECTION

    DRUG FACTS

  • Active Ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antiseptic

  • Uses

    Kills 99.99 % germs and moisturizes 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

    IDLife

    SANITIZE+
    MOISTURIZING HAND SANITIZER
    Kills 99.9% OF GERMS PROTECTION UP TO 4 HOURS
    2 fl. oz. (59mL)

    PATENTED FORMULA

    IDLife SANITIZE+ MOISTURIZING HAND SANITIZER Kills 99.9% OF GERMS PROTECTION UP TO 4 HOURS 2 fl. oz. (59mL) PATENTED FORMULA

  • INGREDIENTS AND APPEARANCE
    IDLIFE SANITIZE MOISTURIZING HAND SANITIZER 
    benzalkonium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69243-1111
    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)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SOY PROTEIN (UNII: R44IWB3RN5)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    JOJOBA OIL (UNII: 724GKU717M)  
    SORBIC ACID (UNII: X045WJ989B)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69243-1111-130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/24/2020
    2NDC:69243-1111-244 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/24/2020
    3NDC:69243-1111-359 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/24/2020
    4NDC:69243-1111-4118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/24/2020
    5NDC:69243-1111-5237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/24/2020
    Labeler - Willspeed Technologies LLC (019063540)
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