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:

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

WAG_CC_760025_NasalGel_BOX

SALINE NASAL MOISTURIZING  WALGREENS
sodium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-5557
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE0.9 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-5557-3030 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/13/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/13/2022
Labeler - WALGREENS COMPANY (008965063)

Revised: 1/2022
Document Id: d6bce8d9-dcdc-4800-e053-2995a90a65c1
Set id: d6b8f762-af6e-7a98-e053-2a95a90aced7
Version: 2
Effective Time: 20220129
 
WALGREENS COMPANY