Label: EQUATE PREMIUM SALINE- sodium chloride 0.65% spray

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

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Drug Label Information

Updated September 24, 2024

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  • Drug Facts

  • Active ingredient

    Sodium Chloride 0.65%

  • Purpose

    Nasal Moisturizer

  • Uses

    Provides instant, soothing relief to dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel, and use of decongestants/steroidal sprays.

  • Warnings

    If pregnant or breast feeding,

    ask a health professional before use.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away. The use of this dispenser by more than one person may spread infection.

  • Directions

    Squeeze bottle twice in each nostril as needed or as directed by physician. For children 3 years old and younger, consult a physician before use. For infants, use drop applicaiton. Hold bottle upright for spray, horizontally for stream, and upside down for drop.

  • Other information

    store at room temperature

  • Inactive ingredients

    Benzalkonium Chloride, Benzyl Alcohol, Purified Water, Sodium Phosphate Dibasic, Sodium Phosphate Monobasic

  • Questions or comments?

    1-888-287-1915

  • Principal display panel

    PRINCIPAL DISPLAY PANEL

  • INGREDIENTS AND APPEARANCE
    EQUATE PREMIUM SALINE 
    sodium chloride 0.65% spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-275
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE0.65 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-275-0388 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/30/2024
    Labeler - Walmart Stores, Inc. (051957769)
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