Label: WHITE RAIN FOAMING ANTIBACTERIAL HAND SPRING WATER- benzalkonium chloride liquid

  • NDC Code(s): 52862-615-00
  • Packager: International Wholesale, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 16, 2023

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  • Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.13%

    Purpose

    Antibacterial

  • Uses

    External

    for hand washing to decrease bacteria on the skin.

  • Warnings

    for external use only.

    When using this product 

    avoid contact with eyes. In case of eye contact, flush with water.

    Stop use and consult a doctor if:

    irritation and redness develops.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    Pump into DRY hands. Lather vigorously for at least 15 seconds. Rinse and dry thoroughly.

  • Inactive Ingredients

    Water(Aqua), Lauramine Oxide, Cetrimonium Chloride, Myristamine Oxide, Glycerin, Coco-Glucoside, Glyceryl Oleate, Fragrance(Parfum), Citric Acid, Sodium Chloride, Disodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue No.1, FD&C Red 33.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    WHITE RAIN FOAMING ANTIBACTERIAL HAND SPRING WATER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52862-615
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    MYRISTAMINE OXIDE (UNII: J086PM3RRT)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    GLYCERYL OLEATE (UNII: 4PC054V79P)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52862-615-001 in 1 CASE01/01/2023
    1177 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/01/2023
    Labeler - International Wholesale, Inc. (161872676)
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