SALINE NASAL SPRAY

Manufacturer
ALAINA HEALTHCARE PRIVATE LIMITED
Effective date
2026-07-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
weekly-update
Hydrated at
2026-07-17 21:43:44

Label at a glance#

ProductSALINE NASAL
Active ingredientSODIUM CHLORIDE
Label structure12 sections

Indications and uses

provides moisture to dry nasal passages helps relieve dry, irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel, and use of decongestants/steroidal sprays.

Dosage and administration

The use of this dispenser by more than one person may spread infection. Hold bottle upright for spray, horizontally for stream, and upside down for drop. For children and adults, squeeze bottle twice in each nostril, as often as needed, or as directed by doctor. For infants, use drop application.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride 0.65%

Purpose

OTC - PURPOSE SECTION

Moisturizer

Uses

INDICATIONS & USAGE SECTION

  • provides moisture to dry nasal passages
  • helps relieve dry, irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel, and use of decongestants/steroidal sprays.

Warnings

WARNINGS SECTION

If pregnant or breast feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

The use of this dispenser by more than one person may spread infection.Hold bottle upright for spray, horizontally for stream, and upside down for drop.

For children and adults,squeeze bottle twice in each nostril, as often as needed, or as directed by doctor.

For infants,use drop application.

OTHER SAFETY INFORMATION

Other information:store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride, disodium hydrogen phosphate anhydrous, purified water, sodium acid phosphate.

OTC - QUESTIONS SECTION

Questions or comments?

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by owner of the registered trademark OCEAN ®.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Saline Nasal Spray
Sodium Chloride 0.65%
Relieves dry nasal passages
Soothes dry, stuffy noses
Safe for frequent daily use
Compare to active ingredients in OCEAN ®
1.5 FL OZ (44 mL)

"Image Description""Image Description"

Saline Nasal Spray
Sodium Chloride 0.65%
Relieves dry nasal passages
Soothes dry, stuffy noses
Safe for frequent daily use
Compare to active ingredients in OCEAN ®
3 FL OZ (90 mL)

"Image Description""Image Description"

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73492-28173492-281-04, 73492-281-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-06-23monthly-update2026-07-17 21:35:35

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
SALINE NASALSODIUM CHLORIDEALAINA HEALTHCARE PRIVATE LIMITEDed30a7f9-7132-42da-9bed-63a9b1c80ab22026-07-07WarningsExact identifier
ndc (package): 73492-281-04
ndc (package): 73492-281-09
ndc (product): 73492-281
ndc11 (package): 73492028109
ndc11 (package): 73492028104
spl id: 56038b75-6518-9302-e063-6394a90a0e21
spl set id: ed30a7f9-7132-42da-9bed-63a9b1c80ab2

Reported adverse events (FAERS/openFDA)#

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