Label: MUCINEX FAST-MAX DM MAX AND MUCINEX FAST-MAX NIGHTTIME DM MAX VALUE PACK- dextromethorphan hbr, guaifenesin and triprolidine hcl kit
- NDC Code(s): 63824-019-66, 72854-141-66, 72854-142-26
- Packager: Reckitt Benckiser LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 4, 2026
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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PURPOSE
Purposes
Day:
Dextromethorphan HBr 20 mg.....................................Cough suppressant
Guaifenesin 400 mg........................................................ExpectorantNight:
Dextromethorphan HBr 20 mg...............................................Cough suppressant
Triprolidine HCl 2.5 mg....................................................................Antihistamine -
INDICATIONS & USAGE
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 sleepNight:
■ 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
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. - KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
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 useNight:
■ 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
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INACTIVE INGREDIENT
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 ingredientNight:
ammonium glycyrrhizate, anhydrous citric acid,
carmine, edetate disodium, flavor, glycerin
(soy),maltodextrin, propylene glycol,
purified water, sodium benzoate, sorbitol,
sucralose, xanthan gum - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MUCINEX FAST-MAX DM MAX AND MUCINEX FAST-MAX NIGHTTIME DM MAX VALUE PACK
dextromethorphan hbr, guaifenesin and triprolidine hcl kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72854-142 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72854-142-26 2 in 1 CARTON 07/01/2026 1 1 in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 180 mL Part 2 1 BOTTLE 180 mL Part 1 of 2 MUCINEX FAST-MAX DM MAX
dextromethorphan hydrobromide and guaifenesin solutionProduct Information Item Code (Source) NDC:63824-019 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 20 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 400 mg in 20 mL Inactive Ingredients Ingredient Name Strength 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 Color red Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63824-019-66 180 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 07/18/2012 Part 2 of 2 MUCINEX FASTMAX NIGHTTIME DM MAX
dextromethorphan hydrobromide, triprolidine hydrochloride solutionProduct Information Item Code (Source) NDC:72854-141 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM) TRIPROLIDINE HYDROCHLORIDE 2.5 mg in 20 mL DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 20 mL Inactive Ingredients Ingredient Name Strength 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 Color purple Score Shape Size Flavor CHERRY (ELDERBERRY AND CHERRY) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72854-141-66 1 in 1 CARTON 1 180 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 07/01/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 07/01/2026 Labeler - Reckitt Benckiser LLC (094405024)




