VICKS SINEX - phenylephrine hydrochloride spray 
Procter & Gamble Manufacturing Company

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VICKS®
Sinex®
NASAL SPRAY

Drug Facts

Active ingredient

Phenylephrine HCl 0.5%

Purpose

Nasal decongestant

Uses

temporarily relieves nasal congestion due to

• colds
• hay fever
• upper respiratory allergies

Warnings

Ask a doctor before use if you have

• heart disease
• thyroid disease
• diabetes
• high blood pressure
• trouble urinating due to enlarged prostate gland

When using this product

• do not exceed recommended dosage
• use of this container by more than one person may cause infection
• temporary burning, stinging, sneezing, or increased nasal discharge may occur
• frequent or prolonged use may cause nasal congestion to recur or worsen

Stop use and ask a doctor if

• symptoms persist for more than 3 days

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

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a poison control center right away.

Directions

adults & children 12 yrs. & older	2 or 3 sprays in each nostril without tilting your head, not more often than every 4 hours.
children 2 to under 12 yrs.	ask a doctor
children under 2 yrs.	do not use

Other information

• store at room temperature

Inactive ingredients

benzalkonium chloride, camphor, chlorhexidine gluconate, citric acid, disodium EDTA, eucalyptol, menthol, purified water, tyloxapol

Questions?

1-800-873-8276

www.vicks.com

Dist. by Procter & Gamble,
Cincinnati OH 45202.

PRINCIPAL DISPLAY PANEL - 14.7 mL bottle carton

VICKS®

Sinex®

NASAL SPRAY

For Sinus Relief
Phenylephrine HCl
Nasal Decongestant

With Soothing
Vicks Vapors

See Drug Facts

1/2 FL OZ (14.7 ml)

VICKS SINEX  phenylephrine hydrochloride   spray

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 37000-540 Route of Administration NASAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Phenylephrine Hydrochloride (Phenylephrine) Phenylephrine Hydrochloride 0.0005 g  in 1 mL

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 37000-540-05 1 BOTTLE In 1 CARTON contains a BOTTLE, SPRAY 1 14.7 mL In 1 BOTTLE, SPRAY This package is contained within the CARTON (37000-540-05)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part341	07/30/1993	07/01/2009

Labeler - Procter & Gamble Manufacturing Company (004238200)

Revised: 06/2010Procter & Gamble Manufacturing Company