Label: HEB NASAL- phenylephrine hydrochloride spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 21, 2023

If you are a consumer or patient please visit this version.

  • 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.

    Nasal Spray Phenylephrine Hydrochloride 1%
  • INGREDIENTS AND APPEARANCE
    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 finalpart34103/14/2019
    Labeler - H E B (007924756)