Indications and uses
For the temporary relief of nasal congestion due to: • common cold • hay fever • upper respiratory allergies
H.E.B. Nasal Spray Drug Facts
- Manufacturer
- H E B
- Effective date
- 2026-09-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- daily-update
- Hydrated at
- 2026-09-22 03:02:39
Label at a glance#
Productheb nasal
Active ingredientPHENYLEPHRINE HYDROCHLORIDE
Label structure9 sections
Dosage and administration
• adults and children 12 years of age & older: 2 or 3 sprays in each nostril not more often 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 • container is filled to proper level for best spray action
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Phenylephrine hydrochloride 1%
Purpose
Nasal decongestant
Uses
For the temporary relief of 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 exceed recommended dosage
- do not use for more than 3 days. use only as directed.
- temporary discomfort such as burning, stinging, sneezing or an increase in nasal discharge may occur
- the use of this container by more than one person may spread infection
- frequent or prolonged use may cause nasal congestion to recur or worsen
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 & older: 2 or 3 sprays in each nostril not more often 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
- container is filled to proper level for best spray action
Inactive ingredients
benzalkonium chloride, benzyl alcohol, citric acid, purified water, sodium chloride, sodium citrate
Questions or comments?
1-866-467-2748
Principal Display Panel
Compare to 4-Way® Fast Acting Nasal Spray active ingredient*
NDC 37808-728-30
H.E.B®
Nasal Spray
Phenylephrine Hydrochloride 1 %
Nasal Decongestant
Relief of:
- Nasal Congestion
- Sinus Congestion
- Sinus Pressure
- Swollen Nasal Membranes
1 FL OZ (30mL)
DO NOT USE IF PRINTED SEAL OVER CAP IS TORN OR MISSING
MADE WITH PRIDE & CARE FOR H-E-B®
SAN ANTONIO, TX 78204
H-E-B®
100% GUARANTEE promise
If you aren’t completely pleases with this product, we’ll be happy to replace it or refund your money.
You have our word on it.
Keep this carton for future reference on full labeling.
*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 | 0041220594320 | GTIN-13: 0041220594320 EAN-13: 0041220594320 GTIN-12: 041220594320 UPC-A: 041220594320 GTIN storage (14 digits): 00041220594320 | 648 EL nasal-spray-image.jpg |
DailyMed Product Concepts#
Products#
Every source-derived product name is available through these pages.
- heb nasal
- Phenylephrine hydrochloride
- PHENYLEPHRINE
- BENZALKONIUM CHLORIDE
- BENZYL ALCOHOL
- ANHYDROUS CITRIC ACID
- WATER
- SODIUM CHLORIDE
- SODIUM CITRATE, UNSPECIFIED FORM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 37808-728 | 37808-728-30 |
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 |
|---|---|---|---|
| 7 | 2025-10-03 | full-release | 2026-06-01 01:15:45 |
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 |
|---|---|---|---|---|---|---|
| 403f3d31-a508-1cd9-e063-6394a90a115f | 2cf319cc-bb49-4b7d-bb08-e3346b4a78d4 | 2025-10-03 | Warnings | 2cf319cc-bb49-4b7d-bb08-e3346b4a78d4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.