Label: NASAL SPRAY, 24-7 FOR LIFE- oxymetazoline hydrochloride 0.05% spray

  • NDC Code(s): 66715-5626-4
  • Packager: Lil' Drug Store Products, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 20, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Drug Facts

    ​Drug Facts

  • Active ingredient

    ​Active ingredient

    Oxymetazoline HCl 0.05%

    Purpose

    Purpose

    Nasal decongestant

  • Uses

    ​Uses

    • temporarily relieves 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

    Warnings

    Ask a doctor before use

    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

    ​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

    Stop use and ask a doctor if symptoms persist.

    ​If pregnant or breast-feeding

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    ​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: consult a doctor
    • Shake well before use. To open, rotate cap to align the marks. Squeeze cap on both sides in a counter-clockwise turn and pull off to remove. To spray, hold bottle between thumb at base and nozzle between first and second fingers. without tilting the head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and sniff deeply. Wipe nozzle clean after use and snap cap back onto the bottle.
  • Other information

    Other information

    • store between 20-25°C (68-77°F)
    • retain carton for future reference on full labeling
  • Inactive ingredients

    Inactive ingredients

    benzalkonium chloride, dibasic sodium phosphate, edetate disodium dihydrate, monobasic sodium phosphate, polyethylene glycol, propylene glycol, povidone, purified water

  • Questions or comments?

    ​Questions or comments?

    call toll free 1-877-507-6516

    (M-F 8AM-4:30PM CST)

  • SPL UNCLASSIFIED SECTION

    DISTRIBUTED BY 7-ELEVEN, INC.
    IRVING, TX 75063 WWW.7-ELEVEN.COM

    Satisfaction Guaranteed 1-800-255-0711


    *This product is not manufactured or distributed by
    Bayer Consumer Healthcare LLC, owner of the
    registered trademark Afrin ®.

  • Nasal Spray , Pump, 24/7 for Life by 7-ELEVEN TM - PDP/Package

    [7-ELEVEN logo]

    No Drip

    Pupm

    Nasal Spray

    Oxymetazoline HCl 0.05%

    Nasal Decongestant Relieves:

    • Congestion
    • Allergy Symptoms
    • Common Cold

    12

    HOUR

    Pump Mist

    compare to

    Afrin Original

    active ingredient*

    1 FL OZ

    (30 mL)

    [caduceus]

    [spray nozzle image]

    PDP/PackageBottle Label

  • INGREDIENTS AND APPEARANCE
    NASAL SPRAY, 24-7 FOR LIFE 
    oxymetazoline hydrochloride 0.05% spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5626
    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
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-5626-41 in 1 CARTON04/19/2022
    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 DrugM01204/19/2022
    Labeler - Lil' Drug Store Products, Inc. (093103646)
    Establishment
    NameAddressID/FEIBusiness Operations
    Seaway Pharma117218785manufacture(66715-5626) , analysis(66715-5626) , pack(66715-5626)