MUCUS RELIEF D- guaifenesin, pseudoephedrine hydrochloride tablet, multilayer, extended release 
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HEB Mucus Relief D Drug Facts

Active ingredients (in each extended-release bi-layer tablet)

Guaifenesin 1200 mg

Pseudoephedrine HCl 120 mg

Purposes

Expectorant

Nasal Decongestant

Uses

helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
temporarily relieves nasal congestion due to:
common cold
hay fever
upper respiratory allergies
temporarily restores freer breathing through the nose
promotes nasal and/or sinus drainage
temporarily relieves sinus congestion and pressure

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

heart disease
high blood pressure
thyroid disease
diabetes
trouble urinating due to an enlarged prostate gland
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

you get nervous, dizzy, or sleepless
symptoms do not get better within 7 days, come back or occur with a 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

do not use if printed blister unit is broken or torn
store between 20-25°C (68-77°F)

Inactive ingredients

carbomer homopolymer type B, colloidal silicon dioxide, FD&C yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

Package/Label Principal Display Panel

Compare to Maximum Strength Mucinex® D active ingredients

H-E-B®

Maximum Strength

Mucus Relief D

Guaifenesin 1200 mg

Pseudoephedrine Hydrochloride 120 mg

Extended-Release Bi-Layer Tablets

Expectorant / Nasal Decongestant

• Clears Nasal/Sinus Congestion

• Thins and Loosens Mucus

• Immediate and Extended Release

12 Hours

Actual Size

24 EXTENDED-RELEASE BI-LAYER TABLETS

34g-1f-mucus-relief-d
MUCUS RELIEF D 
guaifenesin, pseudoephedrine hydrochloride tablet, multilayer, extended release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59640-300
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN1200 mg
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE120 mg
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
Product Characteristics
ColorORANGEScoreno score
ShapeOVALSize22mm
FlavorImprint Code L12
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59640-300-624 in 1 CARTON11/30/2023
16 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21440711/30/2023
Labeler - H E B (007924756)

Revised: 12/2023
Document Id: dc794009-5566-4e91-9ad5-d46068d865e3
Set id: 80acd350-7c96-4620-bd7c-848c85f157ed
Version: 2
Effective Time: 20231212
 
H E B