OTC Medication Information: Mucus Dm

MUCUS DM- guaifenesin and dextromethorphan hydrobromide tablet, extended release
Meijer Distribution Inc

Active ingredients (in each extended-release tablet)

Dextromethorphan HBr 60 mg

Guaifenesin 1200 mg

Purposes

Cough suppressant

Expectorant

Uses

helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
temporarily relieves:
cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
the intensity of coughing
the impulse to cough to help you get to sleep

Warnings

Do not use

for children under 12 years of age
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 a doctor before use if you have

persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
cough accompanied by too much phlegm (mucus)

When using this product

do not use more than directed

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

do not crush, chew, or break tablet
take with a full glass of water
this product can be administered without regard for timing of meals
adults and children 12 years and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hours
children under 12 years of age: do not use

Other information

each tablet contains: magnesium 25 mg
do not use if printed foil under cap is broken or missing
store between 20-25° C (68-77° F)

Inactive ingredients

carbomer homopolymer type B, copovidone, D&C yellow #10 aluminum lake, hypromellose, magnesium hydroxide, magnesium stearate, microcrystalline cellulose, silicon dioxide

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

VALUE SIZE

42 EXTENDED-RELEASE TABLETS

Compare to Maximum Strength Mucinex® DM active ingredients

MAXIMUM STRENGTH

mucus DM

Guaifenesin 1200 mg & Dextromethorphan Hydrobromide 60 mg Extended-Release Tablets

EXPECTORANT/COUGH SUPPRESSANT

12 HOUR | Controls Cough

Thins and Loosens Mucus

42 Extended-Release Tablets

actual size

mucus-dm-image
(click image for full-size original)
MUCUS DM
dextromethorphan hbr, guaifenesin tablet, extended release
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-812
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN 1200 mg
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE 60 mg
Inactive Ingredients
Ingredient Name Strength
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)
COPOVIDONE K25-31
D&C YELLOW NO. 10
HYPROMELLOSE, UNSPECIFIED
MAGNESIUM HYDROXIDE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
SILICON DIOXIDE
Product Characteristics
Color YELLOW (light) Score no score
Shape OVAL Size 22mm
Flavor Imprint Code L812
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:41250-812-55 1 BOTTLE in 1 CARTON contains a BOTTLE
1 42 TABLET, EXTENDED RELEASE in 1 BOTTLE This package is contained within the CARTON (41250-812-55)
2 NDC:41250-812-30 1 BOTTLE in 1 CARTON contains a BOTTLE
2 28 TABLET, EXTENDED RELEASE in 1 BOTTLE This package is contained within the CARTON (41250-812-30)
3 NDC:41250-812-66 1 BOTTLE in 1 CARTON contains a BOTTLE
3 14 TABLET, EXTENDED RELEASE in 1 BOTTLE This package is contained within the CARTON (41250-812-66)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA207602 08/08/2018
Labeler — Meijer Distribution Inc (006959555)

Revised: 12/2023 Meijer Distribution Inc

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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