ZICAM INTENSE SINUS RELIEF- oxymetazoline hydrochloride spray 
Church & Dwight Co., Inc.

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Zicam ®Intense Sinus Relief Nasal Spray

Drug Facts

Active ingredient

Oxymetazoline hydrochloride 0.05%

Purpose

Nasal decongestant

Uses

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 nasal congestion to recur or worsen.
  • temporary discomfort such as burning, stinging, sneezing or an increase in nasal discharge may result
  • use of this container by more than one person may spread infection

Stop use and ask a doctor ifsymptoms 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

To use pump:

Other information

Inactive ingredients

aloe barbadensis gel, benzalkonium chloride, benzyl alcohol, disodium EDTA, disodium phosphate, dl-alpha tocopherol, eucalyptol, glycerin, hydroxyethylcellulose, menthol, monosodium phosphate, polysorbate 80, purified water

Questions? Comments?

call 877-942-2626 toll free

www.zicam.com

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton

ZICAM ®

INTENSE
SINUS
RELIEF

OXYMETAZOLINE HCl 0.05%
NASAL DECONGESTANT

12
HOUR
RELIEF

COLDS*ALLERGIES

Maximum Strength
Relief of Sinus
Pressure

No-Drip Liquid ®
NASAL SPRAY

Cooling
Menthol & Eucalyptus

0.50 FL OZ (15 mL)

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton
ZICAM INTENSE SINUS RELIEF 
oxymetazoline hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-471
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
EUCALYPTOL (UNII: RV6J6604TK)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10237-471-151 in 1 CARTON02/28/2022
115 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01202/28/2022
Labeler - Church & Dwight Co., Inc. (001211952)

Revised: 11/2024
Document Id: 27511a53-c53e-8231-e063-6294a90ad71f
Set id: d916f7ff-84b7-57ef-e053-2995a90a3efa
Version: 3
Effective Time: 20241119
 
Church & Dwight Co., Inc.