Label: NO DRIP NASAL MIST- oxymetazoline spray liquid

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 4, 2023

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  • Drug Facts

    Active Ingredient
    Oxymetazoline Hydrochloride 0.05%

  • Purpose

    Nasal Decongestant

  • Uses

    Temporarily relieves nasal congestion due to:

    • common cold
    • hay fever
    • upper respiroty allergies
    • temporarily relieves sinus congestion and pressure
    • Shrinks swollen membranes so you can breathe more freely
  • Warnings

  • Ask a Doctor before use if you have

    • heart diease
    • high blood pressure
    • diabetes
    • thyiod diease
    • trouble urinating due to enlarged rostate gland.
  • When using this product

    • Do not use more than directed
    • do not use for more than three 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 the reach of children

    if swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Before using for the first time, remove the protective cap form the tip and prime the 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 nostrile. Fully depress rim with a firm and even stroke, and sniff deeply.
    • Wipe nozzle clean after use.
    • Adults and children 6 to under 12 years of age (with adult supervision):2 or 3 sprays in each nostril not more 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.
  • Other information

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

    Benzalkonium Chloride, Disodium EDTA, Glycerin, Microcrystalline Cellulose and Carboxymethylcellulose Sodium, Polyethylene Glycol 300, Povidone, Propylene Glycol, Purified Water, Sodium Phosphate Dibasic, Sodium Phosphate Monobasic

  • Questions or Comments ? 1-800-222-1087

  • Principal Panel 0.5 FLOZ Bottle

    Principal Panel 0.5 FLOZ Bottle

    Walgreens  No Drip Nasal Mist 

    Nasal Spray 

    Oxymetazoline HCL 0.05%

    12 hour Nasal Spray

    Net Wt 0.5 FLOZ (15ml)

    Principal Panel 0.5 FLOZ Bottle

    Principal display panel- Carton label

    Principal display panel- Carton labelPrincipal display panel- Carton labelPrincipal display panel- Carton labelWalgreens No Drip Nasal Mist

    Nasal Spray

    Oxymetazoline HCL 0.05%

    12 hour Nasal Spray

    Net Wt 0.5 FLOZ (15ml)

    Principal display panel- Carton label

  • INGREDIENTS AND APPEARANCE
    NO DRIP NASAL MIST 
    oxymetazoline spray liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2303
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    POVIDONE (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-2303-521 in 1 CARTON08/30/2018
    115 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 DrugM01208/30/2018
    Labeler - Walgreens Company (008965063)