Saline Nasal

Manufacturer
Velocity Pharma LLC
Effective date
2021-04-19
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:39:47

Label at a glance#

ProductSaline Nasal 1 fl oz
Active ingredientSODIUM CHLORIDE
Label structure7 sections

Indications and uses

Nasal congestion Removes inhaled irritants (dust, dirt, pollen) Moisturizes dry nasal passages

Dosage and administration

Squeeze twice in each nostril as needed Upright delivers a spray, horizontally a stream, upside down a drop Take care not to aspirate nasal contents back into bottle If spray tip touches nose, rinse with hot water before replacing cap

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride, 2.65%

Purpose

OTC - PURPOSE SECTION

Nasal Wash to flush allergens and dust from Nasal Passages

Uses

INDICATIONS & USAGE SECTION

Nasal congestion
Removes inhaled irritants (dust, dirt, pollen)
Moisturizes dry nasal passages

Warnings

WARNINGS SECTION

Do not use if seal is broken or missing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings

Use of this product by more than one person may spread infection
Contents under pressure
Do not puncture or incinerate
Avoid spraying in eyes

Keep out of reach of children. The use of this dispenser by more than one person may spread infection.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Squeeze twice in each nostril as needed
  • Upright delivers a spray, horizontally a stream, upside down a drop
  • Take care not to aspirate nasal contents back into bottle
  • If spray tip touches nose, rinse with hot water before replacing cap

Inactive ingredients

INACTIVE INGREDIENT SECTION

A hypertonic solution of purified water, potassium phosphate/Sodium
hydroxide buffer, disodium ethylenediaminetetraacetic acid, benzalkonium chloride

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UntitledUntitled

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
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290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
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fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
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ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76168-701-30Saline Nasal1 fl oz30 mL in 1 BOTTLE, SPRAYSPRAY306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76168-701SALINE NASAL 1 FL OZ (SODIUM CHLORIDE 2.65%) SPRAY [VELOCITY PHARMA LLC]6Legacy NDC, 1 package rows20210420_3393c026-b083-42d4-b552-c6fd644c4684.zip

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
76168-70176168-701-30

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
c05435dd-831b-d20b-e053-2a95a90a8d1a3393c026-b083-42d4-b552-c6fd644c46842021-04-19WarningsExact identifier
spl id: c05435dd-831b-d20b-e053-2a95a90a8d1a
spl set id: 3393c026-b083-42d4-b552-c6fd644c4684

Reported adverse events (FAERS/openFDA)#

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