Mucinex Sinus Max Sinus Pressure Severe Congestion

Manufacturer
Reckitt Benckiser LLC
Effective date
2026-05-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:58:02

Label at a glance#

ProductMucinex Sinus Max Sinus Pressure Severe Congestion
Active ingredientOXYMETAZOLINE HYDROCHLORIDE
Label structure11 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Oxymetazoline hydrochloride 0.05%

INDICATIONS & USAGE SECTION

Purpose:

Nasal Decongestant

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

OTC - PURPOSE SECTION

Purpose:

Nasal Decongestant

WARNINGS SECTION


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 SECTION


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.

OTC - PREGNANCY OR BREAST FEEDING SECTION


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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


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

OTHER SAFETY INFORMATION


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

INACTIVE INGREDIENT SECTION


Inactive ingredients
benzalkonium chloride,
benzododecinium chloride,
cetalkonium chloride, dibasic
sodium phosphate anhydrous,
edetate disodium, glycerin,
monobasic sodium phosphate
anhydrous, myristalkonium
chloride, phosphorous pentoxide,
propylene glycol, purified water,
sodium oxide, sorbitol

OTC - QUESTIONS SECTION


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


Dist. by: RB Health (US)
Parsippany NJ 07054-0224

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1000990oxymetazoline HCl 0.05 % Nasal SprayPSN3
1000990oxymetazoline hydrochloride 0.5 MG/ML Nasal SpraySCD3
1000990oxymetazoline hydrochloride 0.05 % Nasal SpraySY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
OXYMETAZOLINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
e67be450-f8e4-4bc1-88bd-1259d379f55fProduct name120210127
c53f3286-4062-4cf5-8355-399519c639a6Product name120170424
a993dfc5-f219-4460-bde6-30dd724d9ef0Product name120160818
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72854-219-11Mucinex Sinus Max Sinus Pressure Severe Congestion22 mL in 1 BOTTLE, PUMPSPRAY223
72854-219-11Mucinex Sinus Max Sinus Pressure Severe Congestion1 in 1 CARTONSPRAY13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72854-21972854-219-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-12-16monthly-update2026-06-03 17:46:06

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mucinex Sinus Max Sinus Pressure Severe CongestionOXYMETAZOLINE HCIReckitt Benckiser LLC2eeafd83-230c-af92-e063-6294a90a984e2026-05-19WarningsExact identifier
ndc (package): 72854-219-11
ndc (product): 72854-219
ndc11 (package): 72854021911
spl id: 522de586-7700-0278-e063-6394a90aa44c
spl set id: 2eeafd83-230c-af92-e063-6294a90a984e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.