Mucinex Fast-Max Nighttime DM MAX

Manufacturer
Reckitt Benckiser LLC
Effective date
2026-10-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-09 01:01:18

Label at a glance#

ProductMucinex Fastmax Nighttime DM MAX
Active ingredientTRIPROLIDINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
(in each 20 mL)

Dextromethorphan HBr 20 mg
Triprolidine HCl 2.5 mg

OTC - PURPOSE SECTION

Purpose:

Dextromethorphan HBr 20 mg..........Cough suppressant
Triprolidine HCl 2.5 mg...............................Antihistamine

INDICATIONS & USAGE SECTION

Uses
■ temporarily relieves:
■ cough due to minor throat and
bronchial irritation as may occur with
the common cold or inhaled irritants
■ the intensity of coughing
■ the impulse to cough to help you get
to sleep
■ runny nose
■ sneezing
■ itching of the nose or throat
■ itchy, watery eyes due to hay fever

WARNINGS SECTION

Warnings
Do not use
■ if you are now taking a prescription
monoamine oxidase inhibitor (MAOI) (certain
drugs for depression, psychiatric, or
emotional conditions, or Parkinson’s disease),
or for 2 weeks after stopping the MAOI drug.
If you do not know if your prescription drug
contains an MAOI, ask a doctor or
pharmacist before taking this product.

Ask a doctor before use if you have
■ glaucoma
■ trouble urinating due to an enlarged prostate
gland
■ a breathing problem such as emphysema or
chronic bronchitis
■ persistent or chronic cough such as occurs
with smoking, asthma, or emphysema
■ cough that occurs with too much phlegm (mucus)

Ask a doctor or pharmacist before use if you
are
taking sedatives or tranquilizers

When using this product
■ do not use more than directed
■ excitability may occur, especially in children
■ marked drowsiness may occur
■ alcohol, sedatives, and tranquilizers may
increase drowsiness
■ avoid alcoholic drinks
■ use caution when driving a motor vehicle or
operating machinery

Stop use and ask a doctor if
■ cough lasts more than 7 days, comes back, or
occurs with fever, rash, or headache that lasts.
These could be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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


Keep out of reach of children.
In case of overdose, get medical help or contact a
Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions
■ do not take more than 4 doses in any
24-hour period
■ measure only with dosing cup provided
■ do not use dosing cup with other products
■ dose as follows or as directed by a doctor
■ adults and children 12 years of age and over:
20 mL in dosing cup provided every 4 hours
■ children under 12 years of age: do not use

OTHER SAFETY INFORMATION

Other information
■ each 20 mL contains: sodium 12 mg
■ store at 20-25°C (68-77°F)
■ do not refrigerate

INACTIVE INGREDIENT SECTION

Inactive ingredients
ammonium glycyrrhizate, anhydrous citric acid,
carmine, edetate disodium, flavor, glycerin (soy),
maltodextrin, propylene glycol, purified water,
sodium benzoate, sorbitol, sucralose, xanthan gum

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

full carton labelfull carton label

back labelback label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130363824005799GTIN-13: 0363824005799
EAN-13: 0363824005799
GTIN-12: 363824005799
UPC-A: 363824005799
GTIN storage (14 digits): 00363824005799
72854-141 back label.jpg
QR code linkQR Codewww.mucinex.com/pages/product-faqs72854-141 back label.jpg

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72854-14172854-141-66

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
12026-03-25weekly-update2026-07-17 21:41:42

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mucinex Fast-Max DM Max and Mucinex Fast-Max Nighttime DM Max Value PackDEXTROMETHORPHAN HBR, GUAIFENESIN AND TRIPROLIDINE HCLReckitt Benckiser LLC4df37cfb-299f-661f-e063-6394a90ab3372026-06-04WarningsExact identifier
ndc (package): 72854-141-66
ndc11 (package): 72854014166
Mucinex Fastmax Nighttime DM MAXDEXTROMETHORPHAN HYDROBROMIDE, TRIPROLIDINE HYDROCHLORIDERB Health (US) LLC4ddfcfef-9ee6-2280-e063-6294a90af0742026-03-25WarningsExact identifier
ndc (package): 72854-141-66
ndc (product): 72854-141
ndc11 (package): 72854014166
spl set id: 4ddfcfef-9ee6-2280-e063-6294a90af074

Reported adverse events (FAERS/openFDA)#

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