Label: CVS SALINE- nasal spray

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

Drug Label Information

Updated August 22, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts Active 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 healthcare 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 ingredient in Ocean®*

    NDC: 69842-438-30

    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:

    CVS Saline Nasal Spray
  • INGREDIENTS AND APPEARANCE
    CVS SALINE 
    nasal spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-438
    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:69842-438-301 in 1 CARTON02/15/2021
    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 DrugM02202/15/2021
    Labeler - CVS PHARMACY (062312574)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!