FAMILY CARE PREMIUM SALINE NASAL (SODIUM CHLORIDE) SOLUTION [UNITED EXCHANGE CORP]

FAMILY CARE PREMIUM SALINE NASAL (SODIUM CHLORIDE) SOLUTION [UNITED EXCHANGE CORP]
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NDC 65923-557-44
Set ID 1e53f68d-88ef-4758-9039-498e4f23257c
Category HUMAN OTC DRUG LABEL
Packager United Exchange Corp
Generic Name
Product Class
Product Number
Application Number PART349
  • ACTIVE INGREDIENT

    Active Ingredient                                         Purpose

    Sodium chloride 0.65%................................Moisturizer

  • PURPOSE

    Uses

    • For dry nasal membranes
  • WARNINGS

    Warnings

    For external use only

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • DO NOT USE

    The use of this dispenser by more than one person may spread infection

  • INDICATIONS & USAGE

    Directions

    • squeeze twice in each nostril as needed
    • upright delivers a spray, horizontally a stream, upside down a drop
  • INACTIVE INGREDIENT

    Inactive Ingredeints

    Benzalkonium chloride, dibasic sodium phosphate, monobasic sodium, phosphate, purified water, sorbitol solution

  • DOSAGE & ADMINISTRATION

    Distributed by:

    United Exchange Corp.

    17211 Valley View Ave.

    Cerritos, CA 90703 USA

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    FAMILY CARE PREMIUM SALINE NASAL  
    sodium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-557
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE0.29 mg  in 44 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65923-557-4444 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34906/02/2014
    Labeler - United Exchange Corp (840130579)

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