MUCINEX FAST-MAX KICKSTART SEVERE COLD AND FLU - RB Health (US) LLC

Manufacturer
RB Health (US) LLC
Effective date
2026-03-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
weekly-update
Hydrated at
2026-07-17 21:41:51

Label at a glance#

ProductMucinex Fast-Max Kickstart Severe Cold and Flu and Mucinex Fast-Max Recharge Nighttime Cold and Flu
Active ingredientPHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, TRIPROLIDINE HYDROCHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
(in each 20 mL)

Day:

Acetaminophen 650mg
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
Phenylephrine HCl 10 mg

Night:

Acetaminophen 650 mg
Dextromethorphan HBr 20 mg
Triprolidine HCl 2.5 mg

OTC - PURPOSE SECTION

Day:

Acetaminophen 650mg.................................Pain reliever/fever reducer
Dextromethorphan HBr 20 mg.....................................Cough suppressant
Guaifenesin 400 mg..............................................................................Expectorant
Phenylephrine HCl 10 mg..........................................................Nasal decongestant

Night:

Acetaminophen 650 mg............................ ...Pain reliever/fever reducer
Dextromethorphan HBr 20 mg....................................Cough suppressant
Triprolidine HCl 2.5 mg................................................Antihistamine

INDICATIONS & USAGE SECTION

Uses


Day:

■ temporarily relieves these common cold and flu symptoms:
■ cough ■ nasal congestion ■ minor aches and pains ■ sore throat
■ headache ■ stuffy nose ■ sinus congestion and pressure
■ temporarily reduces fever
■ helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial
passageways of bothersome mucus and make coughs more productive

Night:

■ temporarily relieves these common cold and flu symptoms:
■ cough ■ minor aches and pains ■ sore throat
■ headache ■ runny nose ■ sneezing
■ itching of the nose or throat ■ itchy, watery eyes due to hay fever
■ temporarily reduces fever
■ controls cough to help you get to sleep

WARNINGS SECTION

Warnings:

Day:

Liver warning: This product contains acetaminophen. Severe liver damage may occur if

you take:
■ more than 6 doses in 24 hours, which is the maximum daily amount
■ with other drugs containing acetaminophen
■ 3 or more alcoholic drinks daily while using this product


Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may
include: ■ skin reddening ■ blisters ■ rash
If a skin reaction occurs, stop use and seek medical help right away.
Sore throat warning: If sore throat is severe, persists for more than 2 days, is
accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a
doctor promptly.

Do not use
■ with any other drug containing acetaminophen (prescription or nonprescription).
If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
■ 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
■ liver disease ■ heart disease ■ diabetes ■ high blood pressure
■ thyroid disease ■ trouble urinating due to an enlarged prostate gland
■ persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis,
or emphysema ■ cough that occurs with too much phlegm (mucus)

Ask a doctor or pharmacist before use if you are taking the blood thinning drug
warfarin

When using this product do not use more than directed

Stop use and ask a doctor if
■ nervousness, dizziness, or sleeplessness occur
■ pain, nasal congestion, or cough gets worse or lasts more than 7 days
■ fever gets worse or lasts more than 3 days
■ redness or swelling is present
■ new symptoms occur
■ cough comes back, or occurs with fever, rash, or headache that lasts. These could
be signs of a serious condition.

Night:

Liver warning: This product contains acetaminophen. Severe liver damage may occur if
you take:
■ more than 4 doses (80 mL) in 24 hours, which is the maximum daily amount for this
product
■ with other drugs containing acetaminophen
■ 3 or more alcoholic drinks daily while using this product


Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may
include: ■ skin reddening ■ blisters ■ rash
If a skin reaction occurs, stop use and seek medical help right away.
Sore throat warning: If sore throat is severe, persists for more than 2 days, is
accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a
doctor promptly.

Do not use
■ with any other drug containing acetaminophen (prescription or nonprescription).
If you are not sure whether a drug contains acetaminophen, ask a doctor or
pharmacist.
■ 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 ■ liver disease ■ 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 the blood thinning drug warfarin
■ 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
■ pain or cough gets worse or lasts more than 7 days
■ fever gets worse or lasts more than 3 days
■ redness or swelling is present
■ new symptoms occur

■ cough comes back or occurs with rash or
headache that lasts. These could be signs
of a serious condition.

DOSAGE & ADMINISTRATION SECTION

Directions

Day:

do not take more than directed (see
Overdose warning)

■ 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 directed (see
Overdose warning)

■ 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

Day/Night:

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

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.


Overdose warning: Taking more than the
recommended dose (overdose) may cause
liver damage. In case of overdose, get
medical help or contact a Poison Control
Center right away. Quick medical attention is
critical for adults as well as for children even
if you do not notice any signs or symptoms.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Day:

ammonium glycyrrhizate, anhydrous citric acid, D&C yellow no.
10, edetate disodium, FD&C blue no. 1, flavors,
glycerin, propylene glycol, purified water, sodium
benzoate, sodium citrate, sorbitol, sucralose,
xanthan gum

Night:

ammonium glycyrrhizate, anhydrous citric acid, D&C
yellow no. 10, edetate disodium, FD&C red no.
40, flavor, glycerin (soy), propylene glycol,
purified water, sodium benzoate, sorbitol
solution, 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-130363824006031GTIN-13: 0363824006031
EAN-13: 0363824006031
GTIN-12: 363824006031
UPC-A: 363824006031
GTIN storage (14 digits): 00363824006031
72854-188 back label.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72854-138-66ML - Milliliter72854-13812a5d25f-5889-428e-9341-9b72ca0ba5b212024-03-12

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72854-18872854-188-26
72854-13872854-138-66
72854-16772854-167-66

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 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 · 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mucinex Fast-Max Recharge Nighttime Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, TRIPROLIDINE HYDROCHLORIDEReckitt Benckiser LLC4bae240c-70ce-e9c2-e063-6394a90a5f3d2026-05-20WarningsExact identifier
ndc (package): 72854-167-66
ndc (product): 72854-167
ndc11 (package): 72854016766
MUCINEX FAST MAX Liquid Cold and Flu Kickstart and MUCINEX Nightshift KickstartACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, TRIPROLIDINE HCIReckitt Benckiser LLCfdb70793-5dd1-0455-e053-6394a90ac6212026-05-19WarningsExact identifier
ndc (package): 72854-138-66
ndc11 (package): 72854013866
Mucinex Fast-Max Kickstart Severe Cold and Flu and Mucinex Fast-Max Recharge Nighttime Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, AND TRIPROLIDINE HCLRB Health (US) LLC4cc490a6-a27a-a25b-e063-6294a90a3a952026-03-11WarningsExact identifier
ndc (package): 72854-138-66
ndc (package): 72854-167-66
ndc (package): 72854-188-26
ndc (product): 72854-188
ndc11 (package): 72854013866
ndc11 (package): 72854018826
ndc11 (package): 72854016766
spl id: 4cc49345-d3b9-80a6-e063-6294a90ae805
spl set id: 4cc490a6-a27a-a25b-e063-6294a90a3a95
Mucinex Fast-Max Kickstart Severe Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDERB Health (US) LLCfda745ca-b486-47ca-e053-6394a90a87c32024-12-23WarningsExact identifier
ndc (package): 72854-138-66
ndc (product): 72854-138
ndc11 (package): 72854013866

Reported adverse events (FAERS/openFDA)#

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