MUCINEX FAST-MAX SEVERE CONGESTION AND COUGH MAXIMUM STRENGTH- dextromethorphan hydrobromide, guaifenesin capsule, liquid filled

Mucinex Fast-Max Severe Congestion and Cough by

Drug Labeling and Warnings

Mucinex Fast-Max Severe Congestion and Cough by is a Otc medication manufactured, distributed, or labeled by RB Health (US) LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

• Active ingredients (in each liquid gel): Purposes
• Dextromethorphan HBr 10 mg:

  Cough suppressant

• Guaifenesin 200 mg: Expectorant

KEEP OUT OF REACH OF CHILDREN

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

PURPOSE

Dextromethorphan HBr 10 mg....Cough suppressant
Guaifenesin 200mg...............................Expectorant

Uses

Uses:

■ 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

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
■ 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.

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

■ do not take more than 12 capsules in any
24-hour period
■ adults and children 12 years of age and over:
take 2 capsules every 4 hours
■ children under 12 years of age: do not use

OTHER SAFETY INFORMATION

■ store at 20-25°C (68-77°F)
■ avoid excessive heat

INACTIVE INGREDIENT

Inactive ingredients
D&C yellow no.10, FD&C blue no. 1, gelatin,
glycerin, hypromellose, lecithin, light mineral oil,
polyethylene glycol, povidone, propylene glycol,
purified water, sorbitol sorbitan solution, titanium
dioxide

QUESTIONS

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

PRINCIPAL DISPLAY PANEL

Fast Dissolving Liquid Gels!

NDC: 72854-126-16

MAXIMUM STRENGTH

MUCINEX®
FAST-MAX ®

INGREDIENTS AND APPEARANCE

MUCINEX FAST-MAX SEVERE CONGESTION AND COUGH  MAXIMUM STRENGTH
dextromethorphan hydrobromide, guaifenesin capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72854-153
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg

Inactive Ingredients
Ingredient Name	Strength
POVIDONE (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GELATIN (UNII: 2G86QN327L)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SORBITOL SOLUTION (UNII: 8KW3E207O2)
HYPROMELLOSES (UNII: 3NXW29V3WO)

Product Characteristics
Color	green	Score	no score
Shape	OVAL	Size	16mm
Flavor		Imprint Code	AR08
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72854-153-16	2 in 1 CARTON	06/01/2024
1		8 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	06/01/2024

Labeler - RB Health (US) LLC (081049410)