Label: NORTHSIDE HOSPITAL HAND SANITIZING- benzalkonium chloride liquid

  • 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 July 7, 2017

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  • Drug FactsActive Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    First Aid Antiseptic

  • Use:

    Antiseptic Cleansing of face, hands and body.

  • Caution: Keep out of reach of children.

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

  • Warnings:

    For external use only. Do not use in or around the eyes.Do not apply over large area of the body.

  • Stop Use

    if irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

  • Directions:

    Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appopriately after single use.

  • Inactive Ingredients:

    Water, Methylchloroisothiazolinone, Methylisothiazolinone

  • NORTHSIDE HOSPITAL - Instant hand sanitizing wipes - product label

    NH

    NORTHSIDE HOSPITAL

    Instant hands sanitizing wipes
    Hand washing reduces Infections

    Latex Free

    1 Pouch

    NDC# 59647-748-01

    See box for full Drug Facts information

    LOT: MN17817      EXP: 05/19

    Made in the USA for: Food Service Resources
    www.fsrfoodservice.com      1 REV 0

    Med-Nap NH handsan

  • INGREDIENTS AND APPEARANCE
    NORTHSIDE HOSPITAL  HAND SANITIZING
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59647-748
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1.7 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59647-748-001000 in 1 CONTAINER07/05/2017
    1NDC:59647-748-011.7 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/05/2017
    Labeler - Med-Nap LLC (079086400)
    Registrant - Med-Nap LLC (079086400)
    Establishment
    NameAddressID/FEIBusiness Operations
    Med-Nap LLC079086400manufacture(59647-748)
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