Indications and 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.
Quality Choice Saline Nasal Spray
- Manufacturer
- QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
- Effective date
- 2025-07-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:08:56
Label at a glance#
ProductQUALITY CHOICE SALINE
Active ingredientSODIUM CHLORIDE
Label structure10 sections
Dosage and administration
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.
Contacts and useful links#
Websitewww.qualitychoice.com
www.qualitychoice.com
www.qualitychoice.comLabel contents#
Full prescribing information#
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?
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.
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83324-341-30 | QUALITY CHOICESALINE | 1 in 1 CARTON | SPRAY | 1 | 1 | |
| 83324-341-30 | QUALITY CHOICESALINE | 89 mL in 1 BOTTLE | SPRAY | 89 | 1 |
Products#
Every source-derived product name is available through these pages.
- QUALITY CHOICE SALINE
- Plus SOOTHING ALOE
- ALOE VERA LEAF
- BENZALKONIUM CHLORIDE
- BENZYL ALCOHOL
- WATER
- SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM
- SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM
- SODIUM CHLORIDE
- CHLORIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 83324-341 | 83324-341-30 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM | GR686LBA74 | IACT |
| SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM | 3980JIH2SW | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| QUALITY CHOICE SALINE | PLUS SOOTHING ALOE | QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) | 4ae4e88a-aaa5-4195-bedc-622fd5cd9394 | 2025-07-30 | Warnings | 83324-341-30 83324-341 83324034130 3b242523-d704-f237-e063-6394a90aa104 4ae4e88a-aaa5-4195-bedc-622fd5cd9394 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.