CLEAR MIST- sodium chloride liquid

Clear Mist by

Drug Labeling and Warnings

Clear Mist by is a Otc medication manufactured, distributed, or labeled by Leosons Overseas Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Sodium chloride 0.65%

Purpose

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

SPL UNCLASSIFIED SECTION

Distributed by:
LEOSONS
10 Maryland Avenue
Albany, New York 12205

PRINCIPAL DISPLAY PANEL - 88 ML Bottle Carton

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

3 FL. OZ. (88ML)

INGREDIENTS AND APPEARANCE

CLEAR MIST 
sodium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69626-0064
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium Chloride (UNII: 451W47IQ8X) (Chloride Ion - UNII:Q32ZN48698, Sodium Cation - UNII:LYR4M0NH37)	Sodium Chloride	6.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69626-0064-8	1 in 1 CARTON	01/01/2016
1		88 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 69626-0064-5	1 in 1 CARTON	01/01/2016
2		44 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part349	01/01/2016

Labeler - Leosons Overseas Corp (148605470)