Aqua Maris Daily Clean

Manufacturer
JGL d. d.
Effective date
2023-07-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:28:58

Label at a glance#

ProductAqua Maris Daily Clean
Active ingredientSODIUM CHLORIDE
Label structure9 sections

Dosage and administration

Spray 1-2 times in each nostril, several times a day (2-6 times), and more often if necessary. Due to its gentle nature, the product is also suitable for everyday use to help maintain clear nasal passages (drug free, non habit-forming, non-addictive).

Storage and handling

Sealed for your protection. Do not use if safety seal is broken or missing. Do not expose to temperaturs exceeding 50°C/122°F. Do not use the product after the expiry date.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient(s)
Sodium chloride, 9.0 mg/ml (seawater derived)

OTC - PURPOSE SECTION

Purpose
Rinses and cleanses nasal passages

Use

INDICATIONS & USAGE SECTION

For maintaining daily hygiene of the nasal cavity and rinsing away bacteria, viruses and impurities from the nose.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Spray 1-2 times in each nostril, several times a day (2-6 times), and more often if necessary.
  • Due to its gentle nature, the product is also suitable for everyday use to help maintain clear nasal passages (drug free, non habit-forming, non-addictive).

WARNINGS

WARNINGS SECTION

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

WHEN USING THIS PRODUCT

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • For hygiene reasons, the product should only be used by one person; do not share it with others.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

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

Do not expose to temperaturs exceeding 50°C/122°F.

Do not use the product after the expiry date.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Purified Water.


Questions or Comments?

00 385 51 546 399

PRINCIPAL DISPLAY PANEL - 50 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PRINCIPAL DISPLAY PANEL - 150 mL

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Products#

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DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82640-170982640-1709-1
82640-170882640-1708-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
002fc872-a867-c724-e063-6394a90a46c0116d0f34-2755-43fd-a6ec-e9e8911d50792023-07-11WarningsExact identifier
spl id: 002fc872-a867-c724-e063-6394a90a46c0
spl set id: 116d0f34-2755-43fd-a6ec-e9e8911d5079

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.