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
- 2025-12-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 01:19:39
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.
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| PHENYLEPHRINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
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#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83324-215-01 | QUALITY CHOICE | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 2 | |
| 83324-215-01 | QUALITY CHOICE | 30 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 30 | 2 |
Products#
Every source-derived product name is available through these pages.
- QUALITY CHOICE
- Phenylephrine Hydrochloride
- BENZALKONIUM CHLORIDE
- BENZYL ALCOHOL
- ANHYDROUS CITRIC ACID
- WATER
- SODIUM CHLORIDE
- SODIUM CITRATE, UNSPECIFIED FORM
- PHENYLEPHRINE
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 |
|---|---|---|
| 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 |
| PHENYLEPHRINE HYDROCHLORIDE | 04JA59TNSJ | 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 | PHENYLEPHRINE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION | 14596551-dd82-46b3-8eb8-e69efaea105b | 2025-12-04 | Warnings | 83324-215-01 83324-215 83324021501 452038a2-29f0-5f3a-e063-6394a90a70a1 14596551-dd82-46b3-8eb8-e69efaea105b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.