Aqua Maris Daily Drug Facts

Aqua Maris Daily by

Drug Labeling and Warnings

Aqua Maris Daily by is a Otc medication manufactured, distributed, or labeled by JGL d. d.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AQUA MARIS DAILY- sodium chloride spray 
JGL d. d.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Aqua Maris Daily

Drug Facts

Active ingredient(s)
Sodium chloride, 10.5 mg/ml (seawater derived)

Purpose
Moisturizes and cleanses nasal passages.

Use

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

DIRECTIONS

• To maintain daily nasal hygiene andcomfort, spray 1 to 2 times in each nostril. This procedure can be repeated several times a day and over a longer period.
• The procedure can be repeated as often as required to obtain the desired result (drug free, non-habit forming, non-addictive).

WARNINGS

• For nasal use only.
• To avoid contamination, do not touch any surfaces with the dispenser tip.
• Keep out of reach and sight of children.

WHEN USING THIS PRODUCT

• Use only as directed.
• Before using the product for the first time, remove the cap and press the pump 2 to 3 times to release the air.
• For hygiene reasons, the product should only be used by one person; do not share it with others.

OTHER INFORMATION

Sealed for your protection. Do not use if safety seal is broken or missing.

No special storage conditions.

Do not use the product after the expiry date.

INACTIVE INGREDIENT

Purified Water.

Questions or Comments?

00 385 51 546 399

PRINCIPAL DISPLAY PANEL

Aqua Maris Daily Sodium Chloride Spray 30mL- NDC: 82640-1710-1 -Container Label

Aqua Maris Daily Sodium Chloride Spray 30mL - NDC: 82640-1710-1 -Label

Aqua Maris Daily Sodium Chloride Spray 30mL - NDC: 82640-1710-1 -Carton Label

AQUA MARIS DAILY 
sodium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82640-1710
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	10.5 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: 82640-1710-1	1 in 1 CARTON	05/06/2022	07/11/2023
1		30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	05/06/2022	07/11/2023

Labeler - JGL d. d. (631240835)

Establishment
Name	Address	ID/FEI	Business Operations
JGL d. d.		631240835	manufacture(82640-1710)

Revised: 7/2023

Document Id: 0030108d-9c38-d304-e063-6394a90a5ce5

34390-5

Set id: 10e74b61-d0eb-4aa1-b27f-c43314cbb822

Version: 4

Effective Time: 20230711