NasalAsalt

Manufacturer
Nasal and Sinus Health, Inc. | Gerolymatos International
Effective date
2011-09-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:29:57

Label at a glance#

ProductNasalAsalt All-Natural Seawater
Active ingredientSodium Chloride
Label structure7 sections

Indications and uses

NasalAsalt ® may be used 2-4 times per day to help provide fast temporary relief from swelling and congestion. Use NasalAsalt ® as a prewash to help clear mucous buildup prior to using other nasal sprays.

Dosage and administration

Tilt head forward, spray 2-3 times in each nostril directing spray upward and outward toward ear and away from center of nose. Blow nose. For best results, see package insert for the Vanderpool Technique™ for a more thorough nasal cleansing procedure or go to the NasalAsalt ® web site for a video demonstration.

Label contents#

Full prescribing information#

USES

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

NasalAsalt® may be used 2-4 times per day to help provide fast temporary relief from swelling and congestion.

Use NasalAsalt® as a prewash to help clear mucous buildup prior to using other nasal sprays.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Tilt head forward, spray 2-3 times in each nostril directing spray upward and outward toward ear and away from center of nose. Blow nose. For best results, see package insert for the Vanderpool Technique™ for a more thorough nasal cleansing procedure or go to the NasalAsalt® web site for a video demonstration.

WARNINGS

WARNINGS SECTION

OTC - WHEN USING SECTION

Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120° F. Recommended storage at room temperature 59-86°F. Avoid direct exposure to sunlight.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - DO NOT USE SECTION

Do not use if tamper-evident seal is missing or torn on cap.

PRECAUTIONS

PRECAUTIONS SECTION

Do not use with children under 6 years of age except as directed by a physician. Use of this dispenser by more than one person may spread infection.

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

INGREDIENTS

Active Ingredient: Seawater 80%

Inactive Ingredient: Purified Water 20% Sterilized solution equivalent to 2.6% NaCl (sea salt)

SPL UNCLASSIFIED SECTION

Distributed by:

Nasal and Sinus Health, Inc., 16 Spring Hill Court, Bluffton, SC 29910. You may report serious side effects to this address.

PRINCIPAL DISPLAY PANEL - 100 mL Canister Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NASAL•ASALT™

ALL NATURAL SEAWATER SOLUTION
HYPERTONIC SALINE
MOISTURIZING
NASAL SPRAY

Targets Nasal
Dryness, Swelling
and Congestion
Caused by:

COLDS
ALLERGIES

Additional Uses:
AS A NASAL CLEANSE AND
PREWASH SOLUTION

  • To Help Clear Mucous Buildup
    Prior to Using Other Nasal Sprays

FOR COMFORT, HYGIENE AND
NASAL & SINUS HEALTH

  • To Soothe and Moisturize
  • To Flush Out Allergens
    and Irritants

The Every Day Nasal Spray™

Preservative Free

3.38 FL OZ (100 mL)

Hypertonic Saline Nasal Spray

Principal Display Panel - 100 mL Canister Carton
Principal Display Panel - 100 mL Canister Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1192857Nasal Asalt 2.6 % Nasal SprayPSN1
1192851sodium chloride 2.6 % Nasal SprayPSN1
1192857sodium chloride 26 MG/ML Nasal Spray [Nasal Asalt]SBD1
1192851sodium chloride 26 MG/ML Nasal SpraySCD1
1192851NaCl 26 MG/ML Nasal SpraySY1
1192857NaCl 26 MG/ML Nasal Spray [Nasal Asalt]SY1
1192857Nasal Asalt 0.444 MEQ/ML Nasal SpraySY1
1192857Nasal Asalt 2.6 % Nasal SpraySY1
1192857Nasal Asalt 26 MG/ML Nasal SpraySY1
1192851sodium chloride 2.6 % Nasal SpraySY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
SODIUM CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52429-123-012020-01-31C16284748780-19d75b9d0-306d-f424-e053-dadaa90a57ceNASAL•ASALT™ ALL NATURAL SEAWATER SOLUTION HYPERTONIC SALINE MOISTURIZING NASAL SPRAY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52429-123-01NasalAsalt All-Natural Seawater100 mL in 1 CANISTERSPRAY1001
52429-123-01NasalAsalt All-Natural Seawater1 in 1 BOXSPRAY11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52429-123NASALASALT (SODIUM CHLORIDE) SPRAY [NASAL AND SINUS HEALTH, INC.]1Legacy NDC, 2 package rows20111101_3f1a03ce-00a9-4491-961d-4acb4a33af8e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Sodium ChlorideACTIVE INGREDIENT451W47IQ8X1
Sodium CationACTIVE MOIETYLYR4M0NH371
waterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52429-12352429-123-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
Sodium Chloride451W47IQ8XACTIB
water059QF0KO0RIACT

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
01df705a-5399-4014-a292-b3e922ba3dee3f1a03ce-00a9-4491-961d-4acb4a33af8e2011-09-26WarningsExact identifier
spl id: 01df705a-5399-4014-a292-b3e922ba3dee
spl set id: 3f1a03ce-00a9-4491-961d-4acb4a33af8e

Reported adverse events (FAERS/openFDA)#

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