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Sunmark Nasal Fast Relief

Dosage form: spray
Labeler: McKesson
NDC Code: 49348-524

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.

McKesson Nasal Spray Drug Facts

Active ingredient

Phenylephrine hydrochloride 1%


Nasal decongestant

  • temporarily relieves nasal congestion due to:
  • common cold
  • hay fever
  • upper respiratory allergies


Ask a doctor before use if you have
  • heart disease
  • diabetes
  • thyroid disease
  • high blood pressure
  • 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. Frequent or prolonged use may cause nasal congestion to come back or get worse.
  • use only as directed
  • 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.

  • adults and children 12 years and over: 2 or 3 sprays in each nostril not more often than every 4 hours
  • children under 12 years: ask a doctor

Use instructions: with head in a normal, upright position, put atomizer tip into nostril. Squeeze bottle with firm, quick pressure while inhaling. Wipe nozzle clean after each use.

Other information
  • store at 20°-25°C (68°-77°F)

Inactive ingredients

benzalkonium chloride, benzyl alcohol, boric acid, sodium borate, water

Principal Display Panel

Compare to 4 Way® Nasal Spray Active Ingredient

Nasal Spray

Fast Relief

Fast Relief of:

Nasal Congestion, Swollen Nasal Membranes, Sinus Congestion & Sinus Pressure

Nasal Decongestant

Phenylephrine HCl 1.0%

Fast Acting

Nasal Spray Carton

phenylephrine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-524
Route of AdministrationNASALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage Description
1NDC:49348-524-721 BOTTLE, SPRAY (BOTTLE) in 1 CARTON
130 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34109/19/2003
Labeler - McKesson (177667227)

Revised: 02/2010

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.