Label: NA-ZONE- sodium chloride lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 November 23, 2010

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  • ACTIVE INGREDIENT

    SODIUM CHLORIDE

  • INACTIVE INGREDIENTS

    BENZALKONIUM CHLORIDE

    DISODIUM EDTA

    DEIONIZED WATER

    SODIUM BICARBONATE

  • PURPOSE

    STERILE SALINE NASAL SPRAY

  • USE

    SAFETY TO USE AS OFTEN AS NEEDED

  • KEEP OUT OF REACH OF CHILDREN

    Enter section text here

  • DIRECTIONS

    DIRECTIONS - WITH BOTTLE UPRIGHT SQUEEZE FIRMLY AND QUICKLY TO ATOMIZE NA-ZONE INTO EACH NOSTRIL.  RELEASE BOTTLE TO VENT AND REPEAT 2 OR 3 TIMES
  • WARNINGS

    STERILITY GUARANTEED UNTIL THE SEAL IS BROKEN.  NO SIDE EFFECTS  ONCE SEAL IS BROKEN USE BY ONLY ONE PERSON IS RECOMMENDED

  • NA-ZONE LABEL

    NA-ZONE STERILE SALINE NASAL SPRAY
    MANUFACTURED FOR SNUVA INC 715 SOUTH BLVD OAK PARK IL 2 FL OZ (59 ml)
    NA-ZONE FRONT

    NA-ZONE BACK


  • INGREDIENTS AND APPEARANCE
    NA-ZONE 
    sodium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58291-0011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE.65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58291-0011-159 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34901/01/1989
    Labeler - Snuva, Inc. (807310008)
    Registrant - Snuva, Inc. (807310008)
    Establishment
    NameAddressID/FEIBusiness Operations
    Snuva, Inc.807310008manufacture
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