Label: SEVERE ANEFRIN- oxymetazoline hydrochloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 19, 2021

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Oxymetazoline hydrochloride 0.05%

  • 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 use more than directed

    • do not use for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasla congestion to recur or worsen. • temporary discomfort such as burning, stinging, sneezing or an increase in nasla 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.

  • 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 Use:

    Shake well before use. Hold white tabs, press grooved area of cap firmly and turn counterclockwise. Before using the firsst time, prime metered pump by depressing pump firmly several times. To spray, hold bottle with thumn 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. Secure cap after use.

  • Questions or comments? 1-800-925-4733.

  • DISTRIBUTED BY: WALGREENS CO. 200 WILMOT RD., DEERFIELD, IL 60015

    100% SATISFACTION GUARANTEED

    walgreens.com ©2020 Walgreen Co.

  • Inactive Ingredients

    Benzalkonium Chloride Solution, Camphor, CArboxymethyl Cellulose Sodium, Cellulose Gum, Disodium EDTA, Disodium Phosphate, Eucalyptol, Glycerin, Menthol, Microcrystalline Cellulose, PEG-6, Povidone, Propylene Glycol, Purified Water, Sodium Phosphate Monobasic

  • Uses

    • temporarily relives nasal congestions due to:

    • common cold • hay fever • upper respiratory allergies

    • temporarily relieves sinus congestgions and pressure

    • shrinks swollen nasal membranes so you can breath more freely

  • PURPOSE

    Nasal Decongestant

  • Severe Anefrin Nasal Spray

    NO DRIP

    MAXIMUM STRENGTH

    12 HOUR

    + MENTHOL

    severe anefrin

  • INGREDIENTS AND APPEARANCE
    SEVERE ANEFRIN 
    oxymetazoline hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2021
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.05 g  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    EUCALYPTOL (UNII: RV6J6604TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MENTHOL, (+)- (UNII: C6B1OE8P3W)  
    PEG-6 STEARATE (UNII: 8LQC57C6B0)  
    CAMPHOR, (-)- (UNII: 213N3S8275)  
    POVIDONE K30 (UNII: U725QWY32X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM PHOSPHATE, DIBASIC, MONOHYDRATE (UNII: BWZ7K44R51)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-2021-151 in 1 BOTTLE, SPRAY02/08/2021
    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 finalpart34102/08/2021
    Labeler - WALGREENS (008965063)