Label: KROGER SPRINGWATER ANTIBACTERIAL- benzalkonium chloride liquid

  • NDC Code(s): 41226-510-11, 41226-510-52
  • Packager: Kroger Company
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 24, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    Helps decrease bacteria on hands.

  • Warnings

    For external use only.

    When using the product

    Avoid contact with eyes. In case of Contact, Flush with Water.

    Keep out of reach of children.

    In case of accidental ingestion, seek medical attention or contact a Poison Control Center immediately.

  • Directions

    • From pump bottle, apply onto wet hands.
    • Lather and rinse thoroughly.
  • Other Information

    Store at room temperature.

  • Inactive Ingredients

    Water (Aqua), Lauramidopropylamine Oxide, Glycerin, Cetrimonium Chloride, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Sulfate, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI42090), Red 33 (CI 17200).

  • PDP-1, NDC- 41226-510-11

    Principal Display Panel

  • PDP-2, NDC- 41226-510-52

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    KROGER SPRINGWATER ANTIBACTERIAL 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41226-510
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE130 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41226-510-11325 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/05/2024
    2NDC:41226-510-521540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/05/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/05/2024
    Labeler - Kroger Company (006999528)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(41226-510)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!