Label: SALINE NASAL MOISTURIZING WALGREENS- sodium chloride gel

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

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Drug Label Information

Updated December 18, 2024

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  • Active Ingredient

    Sodium Chloride 0.9%

    Sterile, Hypertonic Saline Solution,

    Sodium Bicarbonate to adjust pH

  • Purpose

    Nasal moisturizer

  • Uses

    provides moisture to soothe and hydrate dry nasal passages caused by:

    • indoor heat
    • dry climate
    • air travel
    • high altitude
    • oxygen use
    • CPAP machine use
  • Directions

    Adults and children 6 years and over: Use 1-2 sprays in each nostril up to every 2 hours as needed

    Children under 6 years- Consult a physician

  • Warnings

    Warnings

    Stop use and ask a doctor if use is uncomfortable or dryness persists

    Do not use if allergic to any of the ingredients

    Do not use if safety seal is missing or broken

    For nasal use only, do not use for dry mouth

  • Keep out of reach of chlidren.

  • Other Information

    Store in cool dry place and protect from freezing

  • Inactive ingredients

    Purfied Water, allantoin, glycerin, propylene glycol, sodium hyaluronate, benzalkonium chloride as preservative

  • QUESTIONS ?

    1-888-547-5492

  • Saline Nasal Spray product label

    WAG_CC_760025_NasalGel_BOX

  • INGREDIENTS AND APPEARANCE
    SALINE NASAL MOISTURIZING  WALGREENS
    sodium chloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-5557
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE0.9 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-5557-3030 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/13/202212/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/13/202212/31/2024
    Labeler - WALGREENS COMPANY (008965063)
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