MUCINEX FAST-MAX DM MAX AND MUCINEX FAST-MAX NIGHTTIME DM MAX VALUE PACK- dextromethorphan hbr, guaifenesin and triprolidine hcl  
Reckitt Benckiser LLC

----------

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

Active ingredients (in each 20 mL)

Day:
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg

Night:

Dextromethorphan HBr 20 mg
Triprolidine HCl 2.5 mg

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

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

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.

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.

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

Day/Night:

■ each 20 mL contains: sodium 12 mg

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

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

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

Front of comboBack of Combo

carton label

full carton label

MUCINEX FAST-MAX DM MAX AND MUCINEX FAST-MAX NIGHTTIME DM MAX VALUE PACK 
dextromethorphan hbr, guaifenesin and triprolidine hcl kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72854-142
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72854-142-262 in 1 CARTON07/01/2026
11 in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 180 mL
Part 21 BOTTLE 180 mL
Part 1 of 2
MUCINEX FAST-MAX  DM MAX
dextromethorphan hydrobromide and guaifenesin solution
Product Information
Item Code (Source)NDC:63824-019
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BENZOATE (UNII: OJ245FE5EU)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
SORBITOL (UNII: 506T60A25R)  
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
XANTHAN GUM (UNII: TTV12P4NEE)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
Product Characteristics
ColorredScore    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-019-66180 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01207/18/2012
Part 2 of 2
MUCINEX FASTMAX NIGHTTIME DM MAX 
dextromethorphan hydrobromide, triprolidine hydrochloride solution
Product Information
Item Code (Source)NDC:72854-141
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM) TRIPROLIDINE HYDROCHLORIDE2.5 mg  in 20 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SORBITOL (UNII: 506T60A25R)  
CARMINIC ACID (UNII: CID8Z8N95N)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
XANTHAN GUM (UNII: TTV12P4NEE)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
ColorpurpleScore    
ShapeSize
FlavorCHERRY (ELDERBERRY AND CHERRY) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72854-141-661 in 1 CARTON
1180 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01207/01/2026
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01207/01/2026
Labeler - Reckitt Benckiser LLC (094405024)

Revised: 6/2026
Document Id: 53702759-a205-6d26-e063-6394a90a4843
Set id: 4df37cfb-299f-661f-e063-6394a90ab337
Version: 3
Effective Time: 20260604
 
Reckitt Benckiser LLC