MUCUS RELIEF DM
- Manufacturer
- RITE AID | TIME CAP LABORATORIES, INC.
- Effective date
- 2021-12-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:46:12
Label at a glance#
ProductMUCUS RELIEF DM
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Label structure11 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients (in each immediate-release tablet)
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
OTC - PURPOSE SECTION
Purpose
Cough suppressant
Expectorant
INDICATIONS & USAGE SECTION
Uses
- helps loosen phlegm (mucus)
- helps thin bronchial secretions to make coughs more productive
- temporarily relieves cough due to minor throat and bronchial irritation associated with the common cold
WARNINGS SECTION
Warnings
OTC - DO NOT USE SECTION
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.
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
- cough accompanied by excessive phlegm (mucus)
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
OTC - WHEN USING SECTION
When using the product
- do not exceed recommended dosage
- do not use for more than 7 days
OTC - STOP USE SECTION
Stop use and ask a doctor if
- cough lasts for more than 7 days, recurs, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a healthcare professional 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
- adults and children 12 years of age and older: take 1 tablet every 4 hours with a full glass of water while symptoms persist. Do not exceed 6 doses in 24 hours.
- children under 12 years of age: do not use
OTHER SAFETY INFORMATION
Other information
- store at 25°C (77°F) excursions permitted between 15°-30°C (59°-86°F)
- keep in a dry place and do not expose to excessive heat
INACTIVE INGREDIENT SECTION
Inactive ingredients colloidal silicon dioxide, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone, silicon dioxide, sodium starch glycolate, stearic acid
OTC - QUESTIONS SECTION
Questions or comments?
Call 1-877-290-4008
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
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 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 4fe95224-f543-4dbb-9445-8cca122b48c8 | Product name | 1 | 20150609 |
| e8718272-64cb-4436-969b-176c3067c8f4 | Product name | 1 | 20150609 |
| 106ff02a-57e1-4c4c-a307-fd582ff4e311 | Product name | 1 | 20150212 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 11822-7894-3 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-a768-d83d-e063-dadaa90ab31f | 280R Rite aid 11822 7894 Mucus Relief DM |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11822-7894-3 | MUCUS RELIEF DM | 30 in 1 CARTON | TABLET | 30 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11822-7894 | MUCUS RELIEF DM (DEXTROMETHORPHAN HYDROBROMIDE/GUAIFENESIN) TABLET [RITE AID] | 2 | Legacy NDC, 1 package rows | 20220101_bdbca32c-0c22-70aa-e053-2995a90a82ca.zip |
Products#
Every source-derived product name is available through these pages.
- MUCUS RELIEF DM
- DEXTROMETHORPHAN HYDROBROMIDE/GUAIFENESIN
- CELLULOSE, MICROCRYSTALLINE
- POVIDONE
- MALTODEXTRIN
- DEXTROMETHORPHAN HYDROBROMIDE
- DEXTROMETHORPHAN
- SILICON DIOXIDE
- MAGNESIUM STEARATE
- GUAIFENESIN
- STEARIC ACID
- SODIUM STARCH GLYCOLATE TYPE A POTATO
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 11822-7894 | 11822-7894-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CELLULOSE, MICROCRYSTALLINE | OP1R32D61U | IACT |
| POVIDONE | FZ989GH94E | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| DEXTROMETHORPHAN HYDROBROMIDE | 9D2RTI9KYH | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| GUAIFENESIN | 495W7451VQ | ACTIB |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | 5856J3G2A2 | IACT |
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 |
|---|---|---|---|---|---|---|
| d46bcc0f-2ab6-9fa6-e053-2a95a90ae5a6 | bdbca32c-0c22-70aa-e053-2995a90a82ca | 2021-12-30 | Warnings | d46bcc0f-2ab6-9fa6-e053-2a95a90ae5a6 bdbca32c-0c22-70aa-e053-2995a90a82ca |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.