MUCOSAN SEVERE MULTI-SYMPTOM- dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid

Mucosan Severe Multi-Symptom by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients (in each 20 mL) Purpose

Dextromethorphan HBr, 20 mg...........................Cough suppressant

Guaifenesin, 400 mg..........................................Expectorant

Phenylephrine HCl, 10 mg.................................Nasal decongestant

PURPOSE

Purposes

Cough suppressant

Expectorant

Nasal descongestant

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 bronquial irritation.

WARNINGS

Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional condition, 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, chronic 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 health prefessional 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 strenght product is not intended for use in children under 12 years of age
• measure only wih doisng cup provided
• keep dosing cup with product
• mL=milliliter

• age: dose
• adults and children 12 years of age and older: 20 mL every 4 hours
• children under 1 years of age: do not use

OTHER SAFETY INFORMATION

Other information

• each (20mL) dose contains: sodium 10 mg
• store between 15-30°C (59-86°F)
• do not refrigerate.

INACTIVE INGREDIENT

Inactive ingredients

anhydrous citric acid, edetate disodium, FD&C blue #1, FD&C red #40, flavors, glycerin, propylene glycol, propyl gallate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum.

QUESTIONS

Questions or comments?

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MUCOSAN SEVERE MULTI-SYMPTOM 
dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53145-697
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	10 mg  in 20 mL
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPYL GALLATE (UNII: 8D4SNN7V92)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SORBITOL (UNII: 506T60A25R)
FD&C RED NO. 40 (UNII: WZB9127XOA)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53145-697-06	1 in 1 CARTON	11/01/2024
1		177 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)