Walgreens Saline Nasal Gel

Saline Nasal moisturizing by

Drug Labeling and Warnings

Saline Nasal moisturizing by is a Otc medication manufactured, distributed, or labeled by WALGREENS COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SALINE NASAL MOISTURIZING WALGREENS- sodium chloride gel 
WALGREENS COMPANY

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Walgreens Saline Nasal Gel

Active Ingredient

Sodium Chloride 0.9%

Sterile, Hypertonic Saline Solution,

Sodium Bicarbonate to adjust pH

Purpose

Nasal moisturizer

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

Directions

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

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

Keep out of reach of chlidren.

Other Information

Store in cool dry place and protect from freezing

Inactive ingredients

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

QUESTIONS ?

1-888-547-5492

Saline Nasal Spray product label

SALINE NASAL MOISTURIZING  WALGREENS
sodium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-5557
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	0.9 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-5557-30	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/13/2022	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/13/2022	12/31/2024

Labeler - WALGREENS COMPANY (008965063)

Revised: 12/2024

Document Id: 29915354-4676-7444-e063-6294a90a0fd1

34390-5

Set id: d6b8f762-af6e-7a98-e053-2a95a90aced7

Version: 3

Effective Time: 20241218