Label: PUBLIX EXTRA MOISTURIZING- oxymetazoline hydrochloride spray

  • NDC Code(s): 41415-720-30
  • Packager: PUBLIX SUPER MARKETS, INC
  • Category: HUMAN OTC DRUG LABEL

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:
    ▪
    common cold
    ▪
    hay fever
    ▪
    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

    Shake well before use: Push down cap while turning counterclockwise and remove cap. Remove clip under rim. Before using the first time, prime metered pump by depressing pump firmly several times. To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and sniff deeply. Wipe nozzle clean after use. Replace clip under rim and secure cap after use.

  • Other information

    •
    store at room temperature

    How to use:

    Push down cap while turning counterclockwise and remove cap. Remove clip under rim. Secure cap after use.

  • Inactive ingredients

    benzalkonium chloride, benzyl alcohol, edetate disodium, glycerin, microcrystalline cellulose and carboxymethyl cellulose sodium, polyethylene glycol, povidone, purified water, sodium phosphate dibasic, sodium phosphate monobasic, xanthan gum.

  • Questions or comments?

    1-888-267-3037

  • Principal Display Panel

    Publix®

    NDC# 41415-720-30

    *Compare to the active ingredient in Afrin® No Drip Extra Moisturizing

    EXTRA MOISTURIZING

    nasal mist

    NASAL DECONGESTANT

    OXYMETAZOLINE HCL 0.05%

    12 HOUR PUMP MIST WON’T DRIP FROM NOSE OR DOWN THROAT

    •
    Soothes & helps rehydrate dry noses
    •
    Fast & effective congestion relief
    •
    12 hour relief

    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

    1-888-267-3037 publix.com

    PUBLIX GUARANTEE: COMPLETE SATISFACTION OR YOUR MONEY BACK

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

    Extra MOISTURIZING NASAL MIST
  • INGREDIENTS AND APPEARANCE
    PUBLIX EXTRA MOISTURIZING 
    oxymetazoline hydrochloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41415-720
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)  
    SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41415-720-301 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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