Label: PUBLIX MAXIMUM STRENGTH- oxymetazoline hydrochloride spray

  • NDC Code(s): 41415-715-30
  • Packager: PUBLIX SUPER MARKETS, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 29, 2024

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  • Active ingredient

    Oxymetazoline hydrochloride 0.05%

  • Purpose

    Nasal Decongestant

  • Uses

    ▪
    for the temporarily relief of nasal congestion due to the, common cold, hay fever or other upper respiratory allergies
    ▪
    temporarily relieves sinus congestion and pressure
    ▪
    shrinks swollen nasal membranes so you can breathe more freely
  • Warnings

  • Ask a doctor before use if you have

    ▪
    heart disease
    ▪
    high blood pressure
    ▪
    diabetes
    ▪
    thyroid disease
    ▪
    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
    ▪
    use of this container by more than one person may spread infection
  • 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 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period.
    ▪
    children under 6 years of age: ask a doctor

    To Spray: squeeze bottle quickly and firmly. Do not tilt head backward while spraying. Wipe nozzle clean after use. Secure cap after use.

  • Other information

    ▪
    store at room temperature
  • Inactive ingredients

    benzalkonium chloride, benzyl alcohol, edetate disodium, polyethylene glycol, povidone, propylene glycol, purified water, sodium phosphate dibasic, sodium phosphate monobasic.

  • Questions or comments?

    1-866-467-2748

  • Principal Display Panel

    Publix®

    NDC# 41415-715-30

    Compare to the active ingredient in Afrin® original*

    ORIGINAL

    Nasal Spray

    NASAL DECONGESTANT

    OXYMETAZOLINE HCL 0.05%

    12 HOUR RELIEF

    MAXIMUM STRENGTH

    •
    Fast, Powerful Congestion Relief
    •
    For Colds & Allergies

    1 FL OZ (30 mL)

    IMPORTANT: Keep this carton for future reference on full labeling.

    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.

    *This product is not manufactured or distributed by Bayer Healthcare LLC, distributer of Afrin® Original.

    Original Nasal Spray NASAL DECONGESTANT OXYMETAZOLINE
  • INGREDIENTS AND APPEARANCE
    PUBLIX  MAXIMUM STRENGTH
    oxymetazoline hydrochloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41415-715
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.05 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)  
    SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41415-715-301 in 1 CARTON05/16/2019
    130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/16/2019
    Labeler - PUBLIX SUPER MARKETS, INC (006922009)
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