NASAL SPA NATURAL SEA SALT- sodium chloride spray

Nasal Spa by

Drug Labeling and Warnings

Nasal Spa by is a Otc medication manufactured, distributed, or labeled by NACUR HEALTHCARE LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient:

Natural Sea Salt 9.5 mg/mL

PURPOSE

Purpose

Nasal Moisturizer

INDICATIONS & USAGE

Uses

-For cleansing and moisturizing the nose

-Helps dry nasal congestion caused by

allergens, irritants, colds, occupational and

environmental pollutants

WARNINGS

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

Keep out of reach of children

DOSAGE & ADMINISTRATION

Directions

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

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

DESCRIPTION

Other Information

-Store below 25C (77F)

-Suitable for children and

adults

INACTIVE INGREDIENT

Inactive Ingredient

Purified water

DESCRIPTION

For expiry date see top lid.

Use Nasal Spa Nasal Spray

to help:

• nasal congestion
• dry nose
• runny clear mucus
• rinse out allergens and pollutants
• remove excess mucus
• dripping sensation in the back of the throat
  

DESCRIPTION

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NASAL SPA  NATURAL SEA SALT
sodium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70176-100
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	9.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70176-100-01	1 in 1 CARTON	10/29/2015
1		20 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		10/29/2015

Labeler - NACUR HEALTHCARE LTD (346989317)