HEB NASAL- phenylephrine hydrochloride spray 
H E B

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H.E.B. Nasal Spray Drug Facts

Active ingredient

Phenylephrine hydrochloride 1%

Purpose

Nasal decongestant

Uses

For the temporary relief of nasal congestion due to:

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

Other information

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:

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.

Nasal Spray Phenylephrine Hydrochloride 1%
HEB NASAL 
phenylephrine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-728
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
Product Characteristics
Coloryellow ((Clear to slightly yellow)) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-728-301 in 1 CARTON03/14/2019
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/14/2019
Labeler - H E B (007924756)

Revised: 10/2025
Document Id: 403f3d31-a508-1cd9-e063-6394a90a115f
Set id: 2cf319cc-bb49-4b7d-bb08-e3346b4a78d4
Version: 7
Effective Time: 20251003
 
H E B