AQUA MARIS ISOTONISED- sodium chloride liquid

Aqua Maris Isotonised by

Drug Labeling and Warnings

Aqua Maris Isotonised by is a Otc medication manufactured, distributed, or labeled by JGL North America LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

• Active ingredient Purified Sea Water: Purpose ; Moisturizes and cleanses nasal passages

Uses

For moisturizing and maintaining daily hygiene of the nasal cavity and relieving symptoms of dry and irritated nose

Directions

• Spray into the nostril as needed
• The procedure can be repeated as often as required to obtain the desired result (non-habit forming, non-addicting)

Warnings

• For external use only, do not inject
• Do not use if seal is broken or missing

When using this product

• Use only as directed
• The use of this dispenser by more than one person may spread infection.

Keep out of reach of children

DOSAGE & ADMINISTRATION

Other information

Store between 59° and 77° F (15° to 25°C)

Inactive Ingredient

Purified Water

PRINCIPAL DISPLAY PANEL - 30 ml carton

DAILY

AQUA®
MARIS

100% NATURAL
NASAL SPRAY

DAILY
Irritated &
Dry nose

PRESERVATIVE FREE

1 fl oz (30 ml)

MEDITERRANEAN SEAWATER

INGREDIENTS AND APPEARANCE

AQUA MARIS ISOTONISED 
sodium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76260-101
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	11.25 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: 76260-101-30	1 in 1 CARTON
1		30 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		12/28/2001

Labeler - JGL North America LLC (968070503)