FDA.reportPublic FDA data

Walgreens Saline Nasal Gel

Manufacturer
WALGREENS COMPANY
Effective date
2024-12-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:45:27

Label at a glance#

ProductSaline Nasal moisturizing Walgreens
Active ingredientSODIUM CHLORIDE
Label structure9 sections

Indications and uses

provides moisture to soothe and hydrate dry nasal passages caused by: indoor heat dry climate air travel high altitude oxygen use CPAP machine use

Dosage and administration

Adults and children 6 years and over: Use 1-2 sprays in each nostril up to every 2 hours as needed Children under 6 years- Consult a physician

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride 0.9%

Sterile, Hypertonic Saline Solution,

Sodium Bicarbonate to adjust pH

Purpose

OTC - PURPOSE SECTION

Nasal moisturizer

Uses

INDICATIONS & USAGE SECTION

provides moisture to soothe and hydrate dry nasal passages caused by:

  • indoor heat
  • dry climate
  • air travel
  • high altitude
  • oxygen use
  • CPAP machine use

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years and over: Use 1-2 sprays in each nostril up to every 2 hours as needed

Children under 6 years- Consult a physician

Warnings

WARNINGS SECTION

Warnings

Stop use and ask a doctor if use is uncomfortable or dryness persists

Do not use if allergic to any of the ingredients

Do not use if safety seal is missing or broken

For nasal use only, do not use for dry mouth

Other Information

OTHER SAFETY INFORMATION

Store in cool dry place and protect from freezing

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purfied Water, allantoin, glycerin, propylene glycol, sodium hyaluronate, benzalkonium chloride as preservative

QUESTIONS ?

OTC - QUESTIONS SECTION

1-888-547-5492

Saline Nasal Spray product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WAG_CC_760025_NasalGel_BOXWAG_CC_760025_NasalGel_BOX

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-55570363-5557-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
HYALURONATE SODIUMYSE9PPT4THIACT
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM BICARBONATE8MDF5V39QOIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XACTIB
ALLANTOIN344S277G0ZIACT

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
29915354-4676-7444-e063-6294a90a0fd1d6b8f762-af6e-7a98-e053-2a95a90aced72024-12-18WarningsExact identifier
spl id: 29915354-4676-7444-e063-6294a90a0fd1
spl set id: d6b8f762-af6e-7a98-e053-2a95a90aced7

Reported adverse events (FAERS/openFDA)#

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