Label: GURUNANDA NASAL SALINE- nasal wash powder, for solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated November 26, 2024

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  • Active Ingredients

    Sodium Bicarbonate USP 515mg

    Sodium Chloride USP 1685 mg

  • Purpose

    Nasal Wash

  • Uses

    • Restores vital moisture to provide prompt relief for dry , crusted and inflamed nasal membranes due to chronic sinusitis,colds , low humidity, overuse of nasal decongestant drops and sprays, allergies, minor nose bleeds and other minor nasal irritations.
    • Temporarily relieves nasal stuffiness.
    • Reduces swelling of nasal passages; shrinks swollen membranes.
    • Promotes nasal and/or sinus drainage; temporarily relieves sinus congestion and pressure.
  • Warnings

    • Do not exceed recommended dosage.
    • This product may cause temporary discomfort such as burning , stinging, sneezing or an increase in nasal discharge.
    • The use of this container by more than one person may spread infection.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • Directions

    • Adults and children 4 years and over: Use 1-2 packets per 240 ml upto to every 2 hours as needed
    • Children under 4 years : Consult a Physician
  • Other Information

    • Inspect saline packets for integrity
    • Do not use saline packets if open or torn
    • Protect saline packets from excessive heat and moisture
    • See saline packets oe box for lot# and expiration date
  • Inactive Ingredients

    None

  • PRINCIPAL DISPLAY PANEL

    Principal display panel

  • INGREDIENTS AND APPEARANCE
    GURUNANDA NASAL SALINE 
    nasal wash powder, for solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70708-210
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE0.515 g  in 2.2 g
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE1.685 g  in 2.2 g
    Product Characteristics
    Colorwhite (WHITE CRYSTALLINE GRANULE POWDER) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70708-210-088 in 1 BOX02/12/2024
    12.2 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/12/2024
    Labeler - GURUNANDA LLC (079671169)