Label: KROGER SALINE- nasal spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 19, 2024

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  • Drug FactsActive Ingredients

    Sodium Chloride 0.65%

  • Purpose 

    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 right away at 1-800-222-1222

  • Directions

    For children and adults, squeeze bottle twice in each nostril as often as needed or as directed by physician. For infants, use drop application. Hold bottle upright for spray, horizontally for stream, and upside down for drop. The use of this dispenser by more than one person may spread infection.

  • Other Information

    •
    store at room temperature
  • Inactive Ingredients

    Aloe barbadensis leaf juice (aloe vera gel), benzalkonium chloride, benzyl alcohol, purified water, sodium phosphate dibasic, sodium phosphate monobasic

  • Questions or comments?

    1-866-467-2748

    *This product is not manufactured or distributed by Valeant Pharmaceuticals North America LLC, owners of the registered trademark Ocean®.

    Distributed by:

  • Saline Nasal Spray 

    Compare to the active ingredient in Ocean®*

    NDC: 41226-759-30

    Saline Nasal Spray

    + Soothing Aloe

    Sodium Chloride 0.65%

    •
    Instantly relieves dry nasal passages caused by sinus, cold and allergy medications and dry air
    •
    Gentle enough for infants
    •
    Relief for stuffy noses

    3 FL O.Z. (89 mL)

    TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL AROUND CAP IS BROKEN OR MISSING.

    Distributed by:

    KROGER Saline Nasal Spray
  • INGREDIENTS AND APPEARANCE
    KROGER SALINE 
    nasal spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41226-759
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)  
    SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41226-759-301 in 1 CARTON01/02/2024
    189 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02201/02/2024
    Labeler - KROGER COMPANY (006999528)
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