Label: MUCINEX SINUS MAX SINUS PRESSURE SEVERE CONGESTION- oxymetazoline hci spray
- NDC Code(s): 72854-219-11
- Packager: RB Health (US) LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2025
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
-
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 infectionStop 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.
Wipe nozzle clean after use. To
close, turn cap clockwise.
DO NOT DISCARD CAP.
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MUCINEX SINUS MAX SINUS PRESSURE SEVERE CONGESTION
oxymetazoline hci sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72854-219 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 BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BENZODODECINIUM CHLORIDE (UNII: Y5A751G47H) PHOSPHORUS PENTOXIDE (UNII: 51SWB7223J) CETALKONIUM CHLORIDE (UNII: 85474O1N9D) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) GLYCERIN (UNII: PDC6A3C0OX) MYRISTALKONIUM CHLORIDE (UNII: 0W255OL75T) SODIUM OXIDE (UNII: 3075U8R23D) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITOL (UNII: 506T60A25R) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72854-219-11 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)
