DAYLOGIC FOAMING SANITIZER ALOE (BENZALKONIUM CHLOLRIDE) LIQUID [RITE AID CORPORATION]

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DAYLOGIC FOAMING SANITIZER ALOE (BENZALKONIUM CHLOLRIDE) LIQUID [RITE AID CORPORATION]
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NDC 11822-2440-8
Set ID 2ca9d98d-ac29-4872-8e97-3c46f274199c
Category HUMAN OTC DRUG LABEL
Packager RITE AID CORPORATION
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Active ingredient

    Benzalkonium Chloride 0.1%

    Purpose

    Antiseptic

  • Uses

    to help decrease bacteria on the skin.

  • Warnings

    For external use only

    When using this product

    avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

    Stop use and ask a doctor if

    irritation or redness develops and lasts.

    Keep out of reach of children.

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

  • Directions

    • Pump enough product on your palm to thoroughly cover your hands, rub together until dry.
    • Children under 6 years should be supervised when using this product.
  • Inactive ingredients

    Water (Aqua), Polysorbate 20, Ethylhexyl Methoxycinnamate, Buty Methoxydibenzoylmethane, Ethylhexyl Salicyalte, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Camellia Sinensis Leaf Extract, DMDM Hydantoin, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Yellow 5 (CI 19140).

  • Label copy

    image of the label

  • INGREDIENTS AND APPEARANCE
    DAYLOGIC FOAMING SANITIZER ALOE 
    benzalkonium chlolride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-2440
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    OCTINOXATE (UNII: 4Y5P7MUD51)  
    AVOBENZONE (UNII: G63QQF2NOX)  
    OCTISALATE (UNII: 4X49Y0596W)  
    PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-2440-8237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/20/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/20/2020
    Labeler - RITE AID CORPORATION (014578892)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture(11822-2440)
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