1410 Saline Nasal Spray

Manufacturer: Dynarex Corporation
Effective date: 2026-08-25
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: daily-update
Hydrated at: 2026-08-27 00:01:47

Label at a glance#

ProductSaline

Active ingredientSODIUM CHLORIDE

Label structure10 sections

Dosage and administration

• Hold bottle upright and squeeze firmly for spray. • Hold bottle upside down and squeeze gently for a drop. • Use as often as needed or as directed by a physician. • Wipe nozzle-tip clean after each use.

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-888-396-2739

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride 0.65%

Purpose

OTC - PURPOSE SECTION

Restores Moisture

Use(s)

INDICATIONS & USAGE SECTION

Moisturizes dry, irritated nasal passages due to:

• Colds • Dry air • Smoke • Air travel • Allergies

Warnings

WARNINGS SECTION

• For Nasal use only

•The use of this dispenser by more than one person may spread infection.

Do not use

OTC - DO NOT USE SECTION

• In the eyes. If contact occurs flush with copious amounts of water

• For mouth dryness

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

You are pregnant or breast feeding.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Hold bottle upright and squeeze firmly for spray.

• Hold bottle upside down and squeeze gently for a drop.

• Use as often as needed or as directed by a physician.

• Wipe nozzle-tip clean after each use.

Other Information

OTHER SAFETY INFORMATION

• Store at room temperature between 15°-30°C (59°-86°F)

• Tamper evident. Do not use if seal is torn, cut, or opened.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium Chloride, Benzyl Alcohol, Disodium Phosphate, Sodium Phosphate Monobasic Anhydrous, Water

Questions?

OTC - QUESTIONS SECTION

1-888-396-2739 Monday - Friday 9AM - 5PM EST

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1410 DM MASTER1410 Saline Nasal Spray

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1411 DM MASTER1411 Saline Nasal Spray

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0840117343542	GTIN-13: 0840117343542 EAN-13: 0840117343542 GTIN-12: 840117343542 UPC-A: 840117343542 GTIN storage (14 digits): 00840117343542	1410 DM MASTER (R250120-1).jpg
Barcode	EAN-13	0840117343566	GTIN-13: 0840117343566 EAN-13: 0840117343566 GTIN-12: 840117343566 UPC-A: 840117343566 GTIN storage (14 digits): 00840117343566	1411 DM MASTER (R250120-1).jpg

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Saline
Saline Nasal Spray
SODIUM CHLORIDE
CHLORIDE ION
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS
WATER
DISODIUM PHOSPHATE
BENZALKONIUM CHLORIDE
BENZYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
67777-310	67777-310-01, 67777-310-02, 67777-310-03, 67777-310-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM CHLORIDE	451W47IQ8X	ACTIB
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS	KH7I04HPUU	IACT
WATER	059QF0KO0R	IACT
DISODIUM PHOSPHATE	22ADO53M6F	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
BENZYL ALCOHOL	LKG8494WBH	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Saline	SALINE NASAL SPRAY	Dynarex Corporation	3247ae7d-554f-baab-e063-6294a90aa3ec	2026-08-25	Warnings	Exact identifier ndc (package): 67777-310-03 ndc (package): 67777-310-01 ndc (package): 67777-310-02 ndc (package): 67777-310-04 ndc (product): 67777-310 ndc11 (package): 67777031004 ndc11 (package): 67777031002 ndc11 (package): 67777031003 ndc11 (package): 67777031001 spl id: 59e1efc0-3b88-a73c-e063-6394a90acd02 spl set id: 3247ae7d-554f-baab-e063-6294a90aa3ec

Reported adverse events (FAERS/openFDA)#

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