Mucus Relief DM by Allegiant Health 415- Mucus Relief DM

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]

MUCUS RELIEF DM- dextromethorphan hbr and guaifenesin tablet, film coated 
Allegiant Health

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415- Mucus Relief DM

Active ingredient(s)

Dextromethorphan HBr 20 mg

Guaifenesin 400 mg

Purposes

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

you have

• 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

you are 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

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 children12 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

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

Storage

• store between 20°-25°C (68°- 77°F)

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

Inactive ingredients

croscarmellose sodium, hypromellose, maltodextrin, microcrystalline
cellulose, polyethylene glycol, povidone, silicon dioxide, stearic acid

Questions

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

Principal Display Panel

Mucus Relief DM

MUCUS RELIEF DM 
dextromethorphan hbr and guaifenesin tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69168-415
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)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
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	AH;415
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69168-415-03	150 in 1 BOTTLE; Type 0: Not a Combination Product	12/23/2014	07/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	12/23/2014	07/31/2023

Labeler - Allegiant Health (079501930)

Revised: 11/2020

Document Id: 7474bb77-5ed9-46f2-8448-537e30d431ed

34390-5

Set id: 31a48b97-984c-476a-806b-636653d81b17

Version: 4

Effective Time: 20201104