MUCUS RELIEF DM IMMEDIATE RELEASE- mucus relief dm tablet

Mucus Relief DM by

Drug Labeling and Warnings

Mucus Relief DM by is a Otc medication manufactured, distributed, or labeled by Allegiant Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient(s)

Dextromethorphan HBr 20mg
Guaifenesin 400mg 

Purpose

Cough suppressant
Expectorant

Use(s)

• 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

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

• persistent or chronic cough such as
  occurs with smoking, asthma, chronic
  bronchitis or emphysema

• cough accompanied by too much phlegm (mucus
  

Ask a doctor or pharmacist before use if

taking sedatives or tranquilizers

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

Pregnancy/Breastfeeding

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

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

Directions

Adults and children 12 years 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 information

• store at 25°C (77°F) excursions between 15°-30°C (59°-86°F)

• keep in a dry place and do not expose to heat

• do not use if imprinted safety seal under cap is broken or missing

• You may report side effects to 1-888-952-0050

Inactive ingredients

croscarmellose sodium, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone, silicon dioxide, stearic acid

Questions

Questions or comments?
Call 1-888-952-0050
Monday through Friday 9AM- 5PM EST.

Principal Display Panel

Mucus Relief DM

INGREDIENTS AND APPEARANCE

MUCUS RELIEF DM  IMMEDIATE RELEASE
mucus relief dm tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69168-432
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	20 mg
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	400 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POVIDONE (UNII: FZ989GH94E)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white	Score	2 pieces
Shape	OVAL	Size	16mm
Flavor		Imprint Code	AH432;bisect
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69168-432-98	200 in 1 BOTTLE; Type 0: Not a Combination Product	05/18/2022
2	NDC: 69168-432-07	1 in 1 CARTON	05/18/2022
2		10 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 69168-432-26	1 in 1 CARTON	05/18/2022
3		20 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 69168-432-50	50 in 1 BOTTLE; Type 0: Not a Combination Product	06/08/2022
5	NDC: 69168-432-06	120 in 1 BOTTLE; Type 0: Not a Combination Product	11/06/2023
6	NDC: 69168-432-30	30 in 1 BOTTLE; Type 0: Not a Combination Product	11/06/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	05/18/2022

Labeler - Allegiant Health (079501930)