SALINE NASAL 1 FL OZ- sodium chloride 2.65% spray

Saline Nasal by

Drug Labeling and Warnings

Saline Nasal by is a Otc medication manufactured, distributed, or labeled by ALAINA HEALTHCARE PRIVATE LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Sodium Chloride, 2.65%

Purpose

Nasal Wash to flush allergens and dust from Nasal Passages

Uses

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

Warnings

Do not use if seal is broken or missing.

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 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
• Take care not to aspirate nasal contents back into bottle
• If spray tip touches nose, rinse with hot water before replacing cap

Inactive ingredients

A hypertonic solution of purified water, potassium phosphate/Sodium
hydroxide buffer, disodium ethylenediaminetetraacetic acid, benzalkonium chloride

Label

INGREDIENTS AND APPEARANCE

SALINE NASAL   1 FL OZ
sodium chloride 2.65% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73492-701
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	2.65 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73492-701-30	24 in 1 BOX	11/19/2019
1		30 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
unapproved drug other		11/19/2019

Labeler - ALAINA HEALTHCARE PRIVATE LIMITED (858720927)