Indications and uses
for the temporarily relief nasal congestion due to: • common cold • hay fever • upper respiratory allergies
Quality Choice Nasal Spray Phenylephrine HCl Drug Facts
- Manufacturer
- CHAIN DRUG MARKETING ASSOCIATION
- Effective date
- 2026-10-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- daily-update
- Hydrated at
- 2026-10-30 01:01:58
Label at a glance#
ProductQUALITY CHOICE
Active ingredientPHENYLEPHRINE HYDROCHLORIDE
Label structure9 sections
Dosage and administration
• adults and children 12 years of age and over: 2 or 3 sprays in each nostril not more than every 4 hours • children under 12 years of age: ask a doctor Use instructions: with head in a normal, upright position, put atomizer tip into nostril. Squeeze bottle with firm, quick pressure while inhaling. Wipe nozzle clean after each use.
Storage and handling
• store at room temperature
Contacts and useful links#
Websitewww.qualitychoice.com
www.qualitychoice.com
www.qualitychoice.comLabel contents#
Full prescribing information#
Active ingredient
Phenylephrine hydrochloride 1%
Purpose
Nasal decongestant
Uses
for the temporarily relief nasal congestion due to:
- common cold
- hay fever
- upper respiratory allergies
Warnings
Ask a doctor before use if you have
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- trouble urinating due to an enlarged prostate gland
When using this product
- do not use more than directed
- do not use for more than 3 days.
- Use only as directed.
- Frequent or prolonged use may cause nasal congestion to recur or worsen.
- temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge may occur
- infection may spread if this container is used by more than one person
Stop use and ask a doctor if
symptoms persist
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 (1-800-222-1222).
Directions
- adults and children 12 years of age and over: 2 or 3 sprays in each nostril not more than every 4 hours
- children under 12 years of age: ask a doctor
Use instructions: with head in a normal, upright position, put atomizer tip into nostril. Squeeze bottle with firm, quick pressure while inhaling. Wipe nozzle clean after each use.
Other information
- store at room temperature
Inactive ingredients
benzalkonium chloride, benzyl alcohol, citric acid, purified water, sodium chloride, sodium citrate
Questions or comments?
1-866-467-2748
Principal Display Panel
NDC# 83324-215-01
*Compare to Active Ingredient in 4-Way® Fast Acting Nasal Spray
Nasal Spray
Nasal Decongestant
Phenylephrine Hydrochloride 1%
For Relief of:
Nasal Congestion
Sinus Congestion
Sinus Pressure
Swollen Nasal Membranes
100% QC SATISFACTION GUARANTEED
1 FL OZ (30 mL)
Distributed by: CDMA, Inc.
Novi, MI 48375
Questions: 800-935-2362
*This product is not manufactured or distributed by Novartis Consumer Health, Inc. the owner of the registered trademark 4-Way® Fast Acting Nasal Spray.
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0635515992825 | GTIN-13: 0635515992825 EAN-13: 0635515992825 GTIN-12: 635515992825 UPC-A: 635515992825 GTIN storage (14 digits): 00635515992825 | 390-94-ephrine nose drops.jpg |
| Data code | ITF | 828119 | 390-94-ephrine nose drops.jpg |
DailyMed Product Concepts#
Products#
Every source-derived product name is available through these pages.
- QUALITY CHOICE
- Phenylephrine Hydrochloride
- PHENYLEPHRINE
- BENZALKONIUM CHLORIDE
- BENZYL ALCOHOL
- ANHYDROUS CITRIC ACID
- WATER
- SODIUM CHLORIDE
- SODIUM CITRATE, UNSPECIFIED FORM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 83324-215 | 83324-215-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PHENYLEPHRINE HYDROCHLORIDE | 04JA59TNSJ | ACTIB |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SODIUM CITRATE, UNSPECIFIED FORM | 1Q73Q2JULR | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 2 | 2025-12-04 | full-release | 2026-06-01 01:19:39 |
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 |
|---|---|---|---|---|---|---|
| 452038a2-29f0-5f3a-e063-6394a90a70a1 | 14596551-dd82-46b3-8eb8-e69efaea105b | 2025-12-04 | Warnings | 14596551-dd82-46b3-8eb8-e69efaea105b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.