Label: PUBLIX- phenylephrine hydrochloride spray

  • NDC Code(s): 41415-728-30
  • Packager: PUBLIX SUPER MARKETS, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 7, 2023

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  • 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 at 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?

    1-888-267-3037

  • Principal Display Panel

    Compare to the active ingredient 4-Way® Fast Acting Nasal Spray*

    NDC 41415-728-30

    Publix®

    Nasal Spray

    NASAL DECONGESTANT

    PHENYLEPHRINE HYDROCHLORIDE 1 %

    Fast acting 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

    DISTRIBUTED BY

    PUBLIX SUPER MARKETS, INC.,

    3300 PUBLIX CORPORATE PARKWAY,

    LAKELAND, FL 33811

    publix.com, 1-888-267-3037

    PUBLIX GUARANTEE: COMPLETE SATISFACTION OR YOUR MONEY BACK.

    IMPORTANT: 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.

    Publix Nasal Spray Phenylephrine HCl 1%
  • INGREDIENTS AND APPEARANCE
    PUBLIX 
    phenylephrine hydrochloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41415-728
    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:41415-728-301 in 1 CARTON05/20/2019
    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 DrugM01205/20/2019
    Labeler - PUBLIX SUPER MARKETS, INC (006922009)
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