Mucinex Fast-Max DM Max and Mucinex Fast-Max Nighttime DM Max Value Pack

Manufacturer
Reckitt Benckiser LLC
Effective date
2026-06-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
weekly-update
Hydrated at
2026-07-17 21:41:48

Label at a glance#

ProductMucinex Fast-Max DM Max and Mucinex Fast-Max Nighttime DM Max Value Pack
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, TRIPROLIDINE HYDROCHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients (in each 20 mL)

Day:
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg

Night:

Dextromethorphan HBr 20 mg
Triprolidine HCl 2.5 mg

OTC - PURPOSE SECTION

Purposes

Day:
Dextromethorphan HBr 20 mg.....................................Cough suppressant
Guaifenesin 400 mg........................................................Expectorant

Night:

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

INDICATIONS & USAGE SECTION

Uses

Day:
■ helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial
passageways of bothersome mucus and make coughs more productive
■ 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

Night:

■ 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

Day:
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
■ persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis,
or emphysema
■ cough that occurs with too much phlegm (mucus)


When using this product do not use more than directed


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.

Night:

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

Day:
■ do not take more than 6 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

Night:

■ 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

Day/Night:

■ each 20 mL contains: sodium 12 mg

■ store at 20-25°C (68-77°F)
■ do not refrigerate

INACTIVE INGREDIENT SECTION

Inactive ingredients

Day:
ammonium glycyrrhizate, anhydrous citric acid, edetate disodium, FD&C red no. 40,
flavor, glycerin (soy), propyl gallate, propylene glycol, purified water, sodium benzoate,
sorbitol, sucralose, trisodium citrate dihydrate*, xanthan gum
*may contain this ingredient

Night:

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

Front of comboFront of comboBack of ComboBack of Combo

carton labelcarton label

full carton labelfull carton label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130363824005805GTIN-13: 0363824005805
EAN-13: 0363824005805
GTIN-12: 363824005805
UPC-A: 363824005805
GTIN storage (14 digits): 00363824005805
Toro PDP FInal V2.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63824-019-66ML - Milliliter63824-019de56a7cd-8891-4cd0-ae71-eaa5dcedbeae12014-10-03

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72854-14272854-142-26
63824-01963824-019-66
72854-14172854-141-66

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Source Document#

Source XML

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 · 5 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): 63824-019-66
ndc (package): 72854-142-26
ndc (package): 72854-141-66
ndc (product): 72854-142
ndc11 (package): 63824001966
ndc11 (package): 72854014166
ndc11 (package): 72854014226
spl id: 53702759-a205-6d26-e063-6394a90a4843
spl set id: 4df37cfb-299f-661f-e063-6394a90ab337
Mucinex Fast-Max DM MaxDEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESINReckitt Benckiser LLC6a8cdcad-4881-49b8-a3f1-2c1574300d182026-05-13WarningsExact identifier
ndc (package): 63824-019-66
ndc (product): 63824-019
ndc11 (package): 63824001966
Mucinex Fast-Max DM Max and Mucinex Nighttime Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND TRIPROLIDINE HYDROCHLORIDEReckitt Benckiser LLC3ba2cc08-acad-79a8-e063-6394a90af17f2026-05-13WarningsExact identifier
ndc (package): 63824-019-66
ndc11 (package): 63824001966
Mucinex Fast-Max DM Max and Mucinex Nightshift Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND TRIPROLIDINE HYDROCHLORIDEReckitt Benckiser LLC2ed3c844-0532-40d9-beba-738d196de34d2026-05-13WarningsExact identifier
ndc (package): 63824-019-66
ndc11 (package): 63824001966
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

Reported adverse events (FAERS/openFDA)#

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