Label: NEBUCLEAR MD- saline liquid

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated September 24, 2025

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  • ACTIVE INGREDIENT

    .9% Sodium Chloride

  • PURPOSE

    Saline for Inhalation

  • INDICATIONS & USAGE

    For moistening of the nasal, throat and lungs

  • WARNINGS

    see a doctor if you:

    • Get worse
    • Need more than 12 inhalations in 24 hours
    • Use more than 9 inhalations in 24 hours for 3 or more days a week
    • Ever been hospitalized for asthma
    • Heart disease
    • High blood pressure
    • Diabetes
    • Thyroid disease
    • Seizures
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • Directions

    • Do not use more than directed
    • For use with a Nebulizer.
    • Add 0.5 mL (contents of one vial) of solution to Nebulizer.
  • OTHER SAFETY INFORMATION

    Protect from light. Avoid excessive heat. Protect from freezing.
    Store between 2°C and 25°C (36°F and 77°F).
    How Supplied: NebuClear MD® Saline Solution, .9$ Sodium Chloride, 5mL vials
    20 vials

  • INACTIVE INGREDIENT

    water

  • QUESTIONS

    1 (855) 860-3404

    support@blueechocare.com

    Monday through Friday, 8:00 a.m. to 5:00 p.m. (Pacific Standard Time).

    Manufactured By:


    Blue Echo Care LLC
    3639 SE 21st Ave

    Portland, OR 97202 USA

  • PRINCIPAL DISPLAY PANEL

    Contains 20 NebuClear MD® Saline vials

    NebuClear MD Saline Solution

  • INGREDIENTS AND APPEARANCE
    NEBUCLEAR MD 
    saline liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73117-520
    Route of AdministrationRESPIRATORY (INHALATION)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE9 mg  in 9 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73117-520-1920 mg in 1 BOX; Type 0: Not a Combination Product09/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01209/01/2025
    Labeler - Blue Echo Care LLC (117048847)
    Establishment
    NameAddressID/FEIBusiness Operations
    Blue Echo Care LLC117048847manufacture(73117-520)
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