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.

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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

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

Aqua Maris Daily Sodium Chloride Spray

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

Aqua Maris Daily Sodium Chloride Spray

AQUA MARIS DAILY 
sodium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82640-1710
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE10.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82640-1710-11 in 1 CARTON05/06/2022
130 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34905/06/2022
Labeler - JGL d. d. (631240835)
Establishment
NameAddressID/FEIBusiness Operations
JGL d. d.631240835manufacture(82640-1710)

Revised: 4/2023
Document Id: fa37ce7d-89e2-63e5-e053-6394a90a8958
Set id: 10e74b61-d0eb-4aa1-b27f-c43314cbb822
Version: 3
Effective Time: 20230426
 
JGL d. d.