WALGREENS SALINE MIST EXTRA STRENGTH- sodium chloride spray

Walgreens Saline Mist by

Drug Labeling and Warnings

Walgreens Saline Mist by is a Otc medication manufactured, distributed, or labeled by Walgreen's Corporation, Applied Labs, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Sodium Chloride 3.0%

Sterile, Hypertonic Saline Solution,

Sodium Bicarbonate to adjust pH

Purpose

Nasal Wash

Inactive ingredients

Purfied Water

Uses

• Nasal congestion
• Removes inhaled irritants (dust, dirt, pollen)
• Moisturizes dry nasal passages

Directions

For nasal use only.

Before use, expel a shoet stream of mist into the air. Insert tip of nozzle into one nostril and press down on the textured area at the base of the nozzle so that a gentle mist coats nasal passages. Blow your nose very gently to clear the mucus out. Repeat for the other nostriil.

To flush and irrigate, tilt head to the side over sink. Insert top of nozzle into the top nostril, pressing down on the textured area at the base of the nozzle so that a gentle mist fills sinus passages and flows out the opposite nostril. Repeat in other nostril.

Wipe nozzle after each use.

USE AS OFTEN AS NEEDED

NON-HABIT FORMING

NON-ADDICTING

Warnings

Warnings

• Use of this product by more than one person may spread infection
• Contents under pressure
• Do not puncture or incinerate
• Avoid spraying in eyes

Keep out of reach of chlidren.

• Adults and children 4 years and over: Use as often as needed
• Children under 4 years: Consult a physician

See directions on can for complere instructions

Saline Nasal Spray product label

INGREDIENTS AND APPEARANCE

WALGREENS SALINE MIST  EXTRA STRENGTH
sodium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-1505
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-1505-60	129 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/22/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/22/2019

Labeler - Walgreen's Corporation (008965063)

Establishment
Name	Address	ID/FEI	Business Operations
Applied Labs, Inc.		117337220	manufacture(0363-1505)