MMM - Cough Formula Guaifenesin DM

Manufacturer
Southern Sales & Services, Inc | Southern Sales & Services, Inc.
Effective date
2021-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:28

Label at a glance#

ProductMMM - Cough Formula Guaifenesin DM
Active ingredientGUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE
Label structure10 sections

Storage and handling

Store at room temperature - 15°- 30°C (59°- 86°F) TAMPER-EVIDENT : Do not use if seal under cap is torn, broken or missing.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each 5mI tsp.)
Dextromethorphan HBr USP 10 mg............Cough suppressant

Guaifenesin USP 100mg.............................Expectorant

OTC - PURPOSE SECTION

Expectorant, Cough Suppressant

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 you are taking a prescription drug that contains an MAOI drug, ask a doctor or pharmacist before taking this product.

WARNINGS SECTION

Ask a doctor before use if

you have a cough that lasts or a chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema - cough occurs with too much phlegm (mucus)

Stop use and ask a doctor if

cough lasts for more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signes of a serious condition.

If pregnant or breast-feeding

ask a health professional before use

Keep out of the reach of children

In case of oversdose, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

See DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Do not take more than 6 doses in any 24 hour period

adults and children 12 years and over...10ml (2 teaspoonfuls every 4 hours or as directed by doctor)

Children under 12 years...do not use

STORAGE AND HANDLING SECTION

Store at room temperature - 15°- 30°C (59°- 86°F)

TAMPER-EVIDENT : Do not use if seal under cap is torn, broken or missing.

INACTIVE INGREDIENT SECTION

Propylene glycol, glycerine, citric acid, sucralose, sodium citrate, potassium sorbate, methylparaben, propylparaben, cherry flavor, menthol, FD&C Red#40, purified Water

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

MMM Cough Formula DM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MMM Cough Formula DM

MMM Cough Formula DMMMM Cough Formula DM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
996520dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral SolutionPSN1
996520dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral SolutionSCD1
996520dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral SolutionSY1
996520dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral SolutionSY1
996520dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DEXTROMETHORPHAN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
GUAIFENESIN Pharmacologic Class Indexing1Indexing - Pharmacologic Class20211129

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69822-021-402023-01-30C16284748780-1f386c64a-299c-0266-e053-dadaa90a7c1aMMM Cough Formula Guaifenesin DM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69822-021-40MMM - Cough Formula Guaifenesin DM118 mL in 1 BOTTLELIQUID1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69822-021MMM - COUGH FORMULA GUAIFENESIN DM (GUAIFENESIN DM) LIQUID [SOUTHERN SALES & SERVICES, INC]1Legacy NDC, 1 package rows20210923_cc1fc608-d203-b9eb-e053-2a95a90aa1f5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69822-02169822-021-40

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
cc1fc608-d204-b9eb-e053-2a95a90aa1f5cc1fc608-d203-b9eb-e053-2a95a90aa1f52021-01-01WarningsExact identifier
spl id: cc1fc608-d204-b9eb-e053-2a95a90aa1f5
spl set id: cc1fc608-d203-b9eb-e053-2a95a90aa1f5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.