Label: JABONITO KIDS GREEN APPLE LIQUID- benzalkonium chloride 0.13% liquid

  • NDC Code(s): 62476-009-08
  • Packager: Industria La Popular, S.A.
  • 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 August 4, 2023

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    For washing to 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

    irritation or redness develops - condition persists for more than 72 hours.

    Keep out of reach of children.

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

  • Directions

    Wet hands. Apply palmful to hands. Scrub thoroughly. Rinse thoroughly.

  • Other Information

    Store between 15-30C (59-86F)

  • Inactive Ingredients


    Aqua, Sodium Lauryl Ether Sulfate, Sodium Chloride, Cocamide MEA, Phenoxyethanol, Fragrance (Parfum), Methylchloroisothiazolinone/Methylisothiazolinone, Citric Acid, FD&C Yellow No. 5, FD&C Blue No. 1.

  • Jabonito Kids Green Apple Liquid Hand Soap

    label

  • INGREDIENTS AND APPEARANCE
    JABONITO KIDS GREEN APPLE LIQUID 
    benzalkonium chloride 0.13% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62476-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.31 g  in 237 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SODIUM LAURYL ETHOXYSULFATE (UNII: SUY7YR7K8F)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62476-009-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/01/2023
    Labeler - Industria La Popular, S.A. (846044576)
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