Mucosan Severe Multi-Symptom
- Manufacturer
- Menper Distributors, Inc.
- Effective date
- 2026-01-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 01:31:57
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients (in each 20 mL)Purpose
Dextromethorphan HBr, 20 mg...........................Cough suppressant
Guaifenesin, 400 mg..........................................Expectorant
Phenylephrine HCl, 10 mg.................................Nasal decongestant
OTC - PURPOSE SECTION
Purposes
Cough suppressant
Expectorant
Nasal descongestant
INDICATIONS & USAGE SECTION
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 SECTION
Do not useif 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.
OTC - ASK DOCTOR SECTION
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.
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you aretaking any other oral nasal decongestant or stimulant.
OVERDOSAGE SECTION
Do not exceed recommended dosage.
OTC - STOP USE SECTION
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.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding,ask a health prefessional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.In case of overdose, get medical help or contact a poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
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 SECTION
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.
OTC - QUESTIONS SECTION
Questions or comments?
1-800-560-5223Monday to Friday 9am-4pm, Eastern Time
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1043543 | dextromethorphan HBr 5 MG / guaiFENesin 100 MG / phenylephrine HCl 2.5 MG in 5 mL Oral Solution | PSN | 2 |
| 1043543 | dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution | SCD | 2 |
| 1043543 | dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution | SY | 2 |
| 1043543 | dextromethorphan HBr 5 MG / guaifenesin 100 MG / phenylephrine HCl 2.5 MG per 5 ML Oral Solution | SY | 2 |
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| DEXTROMETHORPHAN Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| GUAIFENESIN Pharmacologic Class Indexing | 1 | Indexing - Pharmacologic Class | 20211129 |
| PHENYLEPHRINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0042279697062 | GTIN-13: 0042279697062 EAN-13: 0042279697062 GTIN-12: 042279697062 UPC-A: 042279697062 GTIN storage (14 digits): 00042279697062 | MUCOSAN SEVERE BOX.jpg |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53145-697-06 | Mucosan Severe Multi-Symptom | 1 in 1 CARTON | LIQUID | 1 | 2 | |
| 53145-697-06 | Mucosan Severe Multi-Symptom | 177 mL in 1 BOTTLE, PLASTIC | LIQUID | 177 | 2 |
Products#
Every source-derived product name is available through these pages.
- Mucosan Severe Multi-Symptom
- DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCL
- FD&C BLUE NO. 1
- GLYCERIN
- EDETATE DISODIUM
- PROPYL GALLATE
- PROPYLENE GLYCOL
- SODIUM BENZOATE
- ANHYDROUS CITRIC ACID
- SORBITOL
- FD&C RED NO. 40
- SUCRALOSE
- XANTHAN GUM
- WATER
- PHENYLEPHRINE HYDROCHLORIDE
- PHENYLEPHRINE
- DEXTROMETHORPHAN HYDROBROMIDE
- DEXTROMETHORPHAN
- GUAIFENESIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53145-697 | 53145-697-06 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| PROPYL GALLATE | 8D4SNN7V92 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| SORBITOL | 506T60A25R | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| WATER | 059QF0KO0R | IACT |
| PHENYLEPHRINE HYDROCHLORIDE | 04JA59TNSJ | ACTIB |
| DEXTROMETHORPHAN HYDROBROMIDE | 9D2RTI9KYH | ACTIB |
| GUAIFENESIN | 495W7451VQ | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Mucosan Severe Multi-Symptom | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Menper Distributors, Inc. | 26a69342-f65f-cb46-e063-6394a90ade10 | 2026-01-08 | Warnings | 53145-697-06 53145-697 53145069706 47e2a389-67b2-5ed2-e063-6294a90aa9c2 26a69342-f65f-cb46-e063-6394a90ade10 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

