YYBA (as PLD) - WELMATE MUCUS RELIEF - DM (MAXIMUM STRENGTH (73581-404)

MUCUS RELIEF - DM by

Drug Labeling and Warnings

MUCUS RELIEF - DM by is a Otc medication manufactured, distributed, or labeled by YYBA CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MUCUS RELIEF - DM MAXIMUM STRENGTH- guaifenesin, dextromethorphan hbr tablet 
YYBA CORP

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YYBA (as PLD) - WELMATE MUCUS RELIEF - DM (MAXIMUM STRENGTH (73581-404)

Active ingredient (in each tablet)

Dextromethorphan Hydrobromide 60 mg
Guaifenesin 1200 mg

Purpose

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 (1-800-222-1222) right away.

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

• store at 20° - 25°C (68° - 77°F)

Inactive ingredients

colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch (maize)

Questions?

call 1-866-933-6337

MUCUS RELIEF - DM  MAXIMUM STRENGTH
guaifenesin, dextromethorphan hbr tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73581-404
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	60 mg
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	1200 mg

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STARCH, CORN (UNII: O8232NY3SJ)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)

Product Characteristics
Color	white (WHITE TO OFF-WHITE)	Score	no score
Shape	OVAL	Size	23mm
Flavor		Imprint Code	X;63
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73581-404-05	50 in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2023
2	NDC: 73581-404-01	100 in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA206941	05/25/2023	04/01/2026

Labeler - YYBA CORP (006339772)

Revised: 4/2026

Document Id: 4f6dcb6e-779b-c3b4-e063-6294a90ae9e7

34390-5

Set id: fc8c9341-6d6f-d194-e053-6294a90ac891

Version: 4

Effective Time: 20260414