Saline Nasal Spray

Saline Nasal Spray

Drug Labeling and Warnings

Drug Details

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SALINE NASAL 1 FL OZ- sodium chloride 2.65% spray 
Velocity Pharma LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Saline Nasal Spray

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

Saline

SALINE NASAL  1 FL OZ
sodium chloride 2.65% spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76168-701
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE2.65 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76168-701-3030 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/19/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/19/2019
Labeler - Velocity Pharma LLC (962198409)

Revised: 11/2019
 
Velocity Pharma LLC


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