EQUATE PREMIUM SALINE- sodium chloride 0.65% spray

EQUATE PREMIUM SALINE by

Drug Labeling and Warnings

EQUATE PREMIUM SALINE by is a Otc medication manufactured, distributed, or labeled by Walmart Stores, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Sodium Chloride 0.65%

Purpose

Nasal Moisturizer

Uses

Provides instant, soothing relief to dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel, and use of decongestants/steroidal sprays.

Warnings

If pregnant or breast feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away. The use of this dispenser by more than one person may spread infection.

Directions

Squeeze bottle twice in each nostril as needed or as directed by physician. For children 3 years old and younger, consult a physician before use. For infants, use drop applicaiton. Hold bottle upright for spray, horizontally for stream, and upside down for drop.

Other information

store at room temperature

Inactive ingredients

Benzalkonium Chloride, Benzyl Alcohol, Purified Water, Sodium Phosphate Dibasic, Sodium Phosphate Monobasic

Questions or comments?

1-888-287-1915

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INGREDIENTS AND APPEARANCE

EQUATE PREMIUM SALINE 
sodium chloride 0.65% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-275
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	0.65 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
WATER (UNII: 059QF0KO0R)
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-275-03	88 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/30/2024

Labeler - Walmart Stores, Inc. (051957769)