DG HEALTH STERILE SALINE MIST- sodium chloride spray

DG Health Sterile Saline Mist by

Drug Labeling and Warnings

DG Health Sterile Saline Mist by is a Otc medication manufactured, distributed, or labeled by DG Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Sodium Chloride 0.9%

Sterile, Hypertonic Saline Solution,

Sodium Bicarbonate to adjust pH

Purpose

Nasal Wash

Uses

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

Directions

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

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.

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.

Other Information

Store between 59 and 86 degree F

Inactive ingredients

Purfied Water

QUESTIONS ?

1-888-547-5492

Saline Nasal Spray product label

INGREDIENTS AND APPEARANCE

DG HEALTH STERILE SALINE MIST 
sodium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-632
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	0.9 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: 55910-632-27	127 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/22/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/22/2023

Labeler - DG Health (068331990)