MUCINEX SINUS MAX CLEAR AND COOL SEVERE CONGESTION- oxymetazoline hci spray

Mucinex Sinus Max Clear and Cool Severe Congestion by

Drug Labeling and Warnings

Mucinex Sinus Max Clear and Cool Severe Congestion by is a Otc medication manufactured, distributed, or labeled by RB Health (US) LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredient
Oxymetazoline hydrochloride 0.05%

PURPOSE

Purpose:

Nasal Decongestant

INDICATIONS & USAGE

Uses
■ temporarily relieves nasal congestion due to:
■ a cold
■ hay fever or other upper respiratory allergies
■ promotes nasal and/or sinus drainage; temporarily
relieves sinus congestion and pressure
■ helps clear nasal passages; shrinks swollen membranes

WARNINGS

Warnings
Ask a doctor before use if you have
■ heart disease

■ high blood pressure
■ thyroid disease

■ diabetes
■ difficulty in urination due to enlargement of the
prostate gland

When using this product
■ do not exceed recommended dosage
■ do not use this product for more than 3 days. Use
only as directed. Frequent or prolonged use may
cause nasal congestion to recur or worsen.
■ this product may cause temporary discomfort such
as burning, stinging, sneezing, or an increase in
nasal discharge
■ the use of this container by more than one person
may spread infection

Stop use and ask a doctor if symptoms persist

DOSAGE & ADMINISTRATION

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: consult a doctor.

Shake well before use.
To open, hold by the white grips then squeeze, push down
firmly and turn cap counterclockwise. Before using for the
first time, remove the protective cap from the tip and
prime metered pump by depressing firmly several times.
To spray, hold bottle with thumb at the base and nozzle
between first and second fingers.Without tilting head,
insert nozzle into nostril. Fully depress pump all the
way down with a firm even stroke and sniff deeply.

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

Inactive ingredients
benzalkonium chloride,
benzododecinium chloride,
camphor, cetalkonium chloride,
colloidal silicon dioxide, edetate
disodium, eucalyptol, glycine,
linoleic acid, linolenic acid,
menthol, myristalkonium
chloride, myristic acid, oleic
acid, palmitic acid, palmitoleic
acid, polyethylene glycol,
polysorbate 80, propylene glycol,
purified water, sodium
carbonate, sodium chloride,
sodium hydroxide, stearic acid

QUESTIONS

Questions?
1-866-MUCINEX (1-866-682-4639)

PREGNANCY OR BREAST FEEDING

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical
help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MUCINEX SINUS MAX CLEAR AND COOL SEVERE CONGESTION 
oxymetazoline hci spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72854-218
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY)	OXYMETAZOLINE HYDROCHLORIDE	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CETALKONIUM CHLORIDE (UNII: 85474O1N9D)
EDETATE DISODIUM (UNII: 7FLD91C86K)
EUCALYPTOL (UNII: RV6J6604TK)
LINOLEIC ACID (UNII: 9KJL21T0QJ)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
MYRISTIC ACID (UNII: 0I3V7S25AW)
OLEIC ACID (UNII: 2UMI9U37CP)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARIC ACID (UNII: 4ELV7Z65AP)
MYRISTALKONIUM CHLORIDE (UNII: 0W255OL75T)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BENZODODECINIUM CHLORIDE (UNII: Y5A751G47H)
CAMPHOR, (-)- (UNII: 213N3S8275)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
GLYCINE (UNII: TE7660XO1C)
PALMITIC ACID (UNII: 2V16EO95H1)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LINOLENIC ACID (UNII: 0RBV727H71)
PALMITOLEIC ACID (UNII: 209B6YPZ4I)
SODIUM CARBONATE (UNII: 45P3261C7T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72854-218-11	1 in 1 CARTON	06/01/2025
1		22 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	06/01/2025

Labeler - RB Health (US) LLC (081049410)