MUCOSAN MULTI-SYMPTOM CHERRY- dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride liquid

Mucosan Multi-Symptom Cherry by

Drug Labeling and Warnings

Mucosan Multi-Symptom Cherry by is a Otc medication manufactured, distributed, or labeled by Menper Distributors, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INACTIVE INGREDIENT

Active ingredients (in each 5 mL or teaspoon) Purpose

Dextromethorphan HBr, 10 mg..............................Cough suppressant

Guaifenesin, 100 mg..............................................Expectorant

Phenylephrine HCl, 5 mg.......................................Nasal decongestant

PURPOSE

Purposes

Cough suppressant

Expectorant

Nasal decongestant

INDICATIONS & USAGE

Uses

• helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
• temporarily relieves these symptoms occuring with a cold:
• nasal congestion
• cough due to minor throat and bronchial irritation

WARNINGS

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 DOCTOR

Ask a doctor before use if you have

• heart disease
• high blood pressure
• thyroid disease
• diabetes
• trouble urinating due to an enlarged prostate gland
• cough that occurs with too much phlegm (mucus)
• cough that lasts or is chronic such as occurs with smoking, asthma, chornic bronchitis or emphysema

ASK DOCTOR/PHARMACIST

Ask a doctor or pharmacist before use if you are

taking any other oral nasal decongestant or stimulant.

OVERDOSAGE

Do not exceed recommended dosage.

STOP USE

Stop use and ask a doctor if

• you get nervous, dizzy or sleepless
• symptoms do not get better within 7 days or are accompanied by fever
• cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistant headache. These could be signs of a serious condition.

PREGNANCY OR BREAST FEEDING

If pregnant or breast - feeding, ask a helath professional before use.

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.

DOSAGE & ADMINISTRATION

Directions

• do not take more than 6 doses in any 24 hour period
• this adult stregth product is not intended for use in children under 12 years of age
• measure only with dosing cup provided
• keep dosing cup with product
• TSP=teaspoon

• age: dose
• adults and children 12 years and over: 2 teaspoons (10mL) every 4 hours
• children under 12 years: do not use

OTHER SAFETY INFORMATION

Ohter information

• each teaspoon (5mL) contains: sodium 3 mg
• store at 15-30°C (59-86°F). Do not refrigetate.

INACTIVE INGREDIENT

anhydrous citric acid, FD&C red #40, flavor, glycerin, menthol, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose

QUESTIONS

Questions or comments?

1-800-560-5223 Monday to Friday 9am-4pm, Eastern Time

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MUCOSAN MULTI-SYMPTOM CHERRY 
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53145-693
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  in 5 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	5 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	100 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCERIN (UNII: PDC6A3C0OX)
FD&C RED NO. 40 (UNII: WZB9127XOA)
MENTHOL (UNII: L7T10EIP3A)
SORBITOL SOLUTION (UNII: 8KW3E207O2)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53145-693-04	1 in 1 CARTON	11/01/2024
1		118 mL in 1 BOTTLE, PLASTIC; 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	11/01/2024

Labeler - Menper Distributors, Inc. (101947166)

Registrant - Menper Distributors, Inc. (101947166)