VORTEX MOISTURIZER NASAL- sodium chloride liquid 
Vortex Life Sciences, Inc.

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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Vortex Moisturizer Nasal Spray

Drug Facts

Active Ingredients:

Sodium Chloride 0.65%

Purpose:

Moisturizer

Inactive Ingredient:

Purified mineral water

Uses

Temporary relief of dry irritated nasal passages
Promotes healthy nasal passages
Clears and invigorates breathing

Directions:

Sniff and inhale deeply while spraying into nostril.
12 years old- adult: 3 sprays in each nostril.
6 - 12 years old: 2 sprays in each nostril.
3 - 6 years old: 1 spray in each nostril.
Children under age 3: 1 spray. Consult a
physician.
To use, remove cap, insert the nozzle into
the nostril and depress the pump completely
while sniffing deeply.
Day 1: every 3 hours, minimum 5 doses/day
Day 2: every 3 hours, minimum 5 doses/day
Day 3: 3 times a day.
Day 4: at bedtime.
Day 5: at bedtime.
Day 6 - 9: skip.
Day 10: Final dose at bedtime.
For moderate to severe symptoms every 3 hours (minimum 5 doses/24 hrs) until symptoms have significantly reduced. Then,
resume at day 3 schedule.

WARNING:

Use only as directed.

If pregnant or breastfeeding,

consult with a physician before use.

Keep out of reach of children.

Stop use and consult with a physician

if you experience any discomfort while using this product.

In case of overdose, get medical help or contact a Poison Control Center at 1-800-222-2222 right away.

Other Information:

Store and use at room temperature Inspect bottle for integrity Do not use if safety seal is broken

Package Labeling:

Label

VORTEX MOISTURIZER NASAL 
sodium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82529-000
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82529-000-011 in 1 BOX03/01/2022
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/01/2022
Labeler - Vortex Life Sciences, Inc. (118489121)

Revised: 3/2022
Document Id: d9a1828b-0288-0a20-e053-2a95a90a4838
Set id: d87f20d6-933f-4419-b035-e307a13a60aa
Version: 1
Effective Time: 20220307
 
Vortex Life Sciences, Inc.