AQUA MARIS THROAT- sodium chloride spray

Aqua Maris Throat by

Drug Labeling and Warnings

Aqua Maris Throat 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 ; Relieves symptoms of sore throat

Uses

• For alleviation of sore throat and bad breath resulting from blocked nose or salivary gland diseases
• For maintaining oral hygiene after surgical interventions in the oral cavity, pharynx and after tonsillectomy

Directions

• Turn the dispenser into the horizontal position
• Direct the dispenser towards the throat and apply 3-4 dispersions 4-6 times per day
• The procedure can be repeated as often as required to obtain the desired result

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
• Avoid contamination, do not touch tip of container to any surface
• 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

Throat Spray

AQUA®
MARIS
hypertonic

Adriatic
sea water

30 mle

INGREDIENTS AND APPEARANCE

AQUA MARIS THROAT 
sodium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76260-105
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CATION	37.5 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: 76260-105-30	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		04/20/2005

Labeler - JGL North America LLC (968070503)