NASAL SPA NATURAL SEA SALT- sodium chloride spray 
NACUR HEALTHCARE LTD

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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Drug Facts

Active Ingredient:

Natural Sea Salt 9.5 mg/mL

Purpose

Nasal Moisturizer

Uses

-For cleansing and moisturizing the nose

-Helps dry nasal congestion caused by

allergens, irritants, colds, occupational and

environmental pollutants

Warnings

-Do not share between users  -Do not use after the

expiry date  -Use within 6 months of opening

Keep out of reach of children

Directions

-Spray 2 - 3 times into each nostril and inhale through

your nose  -For best results, use as often as needed

Other Information

-Store below 25C (77F)

-Suitable for children and

adults

Inactive Ingredient

Purified water

For expiry date see top lid.

Use Nasal Spa Nasal Spray

to help:

The patented applicator of

the Nasal Spa Nasal Spray

contains an highly effective

valve and an oligo-

dynamically active silver coil

which protects the solution

and the dosage applied

against microbial

congestion.

The sea salt is manufactured

in a highly technical

process (spray-drying)

harvesting seawater taken

from an archipelago off

the coast of France in Europe.

Compared to standard

sodium chloride solutions,

the gentle, isotonic natural

sea salt solution (0.95%) of

the Nasal Spa Spray is

rich in minerals and trace

elements.

MADE IN GERMANY

copy of label

NASAL SPA  NATURAL SEA SALT
sodium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70176-100
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE9.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70176-100-011 in 1 CARTON10/29/2015
120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/29/2015
Labeler - NACUR HEALTHCARE LTD (346989317)

Revised: 4/2016
Document Id: 64ff8db4-4f08-4120-9c24-fac053c11d08
Set id: faea1d62-be0b-4064-9978-5dacbd282cdc
Version: 4
Effective Time: 20160424
 
NACUR HEALTHCARE LTD