QUALITY CHOICE SALINE- plus soothing aloe spray

QUALITY CHOICE by

Drug Labeling and Warnings

QUALITY CHOICE by is a Otc medication manufactured, distributed, or labeled by QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION). Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active Ingredients

Sodium Chloride 0.65%

Purpose 

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 right away at 1-800-222-1222

Directions

For children and adults,squeeze bottle twice in each nostril as often as needed or as directed by physician. For infants,use drop application. Hold bottle upright for spray, horizontally for stream, and upside down for drop. The use of this dispenser by more than one person may spread infection.

Other Information

• store at room temperature

Inactive Ingredients

Aloe barbadensis leaf juice (aloe vera gel), benzalkonium chloride, benzyl alcohol, purified water, sodium phosphate dibasic, sodium phosphate monobasic

Questions or comments?

1-866-467-2748

Distributed by: CDMA, Inc.

Novi, MI, 48375

www.qualitychoice.com

Questions: 800-935-2362

Saline Nasal Spray 

NDC: 83324-341-30

Saline Nasal Spray

+Soothing Aloe

Sodium Chloride 0.65%

Relief for Stuffy Noses

Gentle Enough for Infants

3 FL OZ (89 mL)

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL AROUND CAP IS BROKEN OR MISSING.

INGREDIENTS AND APPEARANCE

QUALITY CHOICE   SALINE
plus soothing aloe spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83324-341
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	6.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BENZYL ALCOHOL (UNII: LKG8494WBH)
WATER (UNII: 059QF0KO0R)
SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)
SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83324-341-30	1 in 1 CARTON	07/11/2025
1		89 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	07/11/2025

Labeler - QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) (011920774)