Label: CLEAR MIST- sodium chloride liquid

  • NDC Code(s): 69626-0064-5, 69626-0064-8
  • Packager: Leosons Overseas Corp
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 21, 2021

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

View All Sections
  • Drug Facts

    Drug Facts

  • Active ingredient & Purpose

    Active ingredientsPurpose
    Sodium chloride 0.65%Moisturizer
  • Uses

    • For dry nasal membranes
  • Warnings

    Do not use

    • if seal is broken or missing.

    Keep out of reach of children.

    The use of this dispenser by more than one person may spread infection.

  • Directions

    • squeeze twice in each nostril as needed
    • upright delivers a spray, horizontally a stream, upside down a drop
  • Inactive Ingredients

    benzalkonium chloride, disodium phosphate, phenylcarbinol, monosodium phosphate, water.

  • Questions or comments?

    Call toll-free at 1-855-452-9500 or email at info@Leosonsintl.com

  • Distributed by:


    LEOSONS

    10 Maryland Avenue
    Albany, New York 12205

  • PRINCIPAL DISPLAY PANEL

    Clear Mist ®

    Saline

    Nasal

    Spray

    Contains Sodium Chloride 0.65%

    Alcohol Free

    Bottle

    Works 3 Ways

    mist stream drops

    Safe for all ages

    Naturally soothes
    nasal passages

    Principal Display Panel - 88 ML Bottle Carton

  • INGREDIENTS AND APPEARANCE
    CLEAR MIST 
    sodium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69626-0064
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE6.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69626-0064-81 in 1 CARTON01/01/2016
    188 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    2NDC:69626-0064-51 in 1 CARTON01/01/2016
    244 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34901/01/2016
    Labeler - Leosons Overseas Corp (148605470)
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!