Label: MUCUS D- guaifenesin, pseudoephedrine hydrochloride tablet, multilayer, extended release
- NDC Code(s): 51316-345-62
- Packager: CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated February 26, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients (in each extended-release tablet)
- Purposes
-
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)
-
Directions
- •
- do not crush, chew, or break extended-release 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 extended-release tablet every 12 hours; not more than 2 extended-release tablets in 24 hours
- •
- children under 12 years of age: do not use
- Other information
- Inactive ingredients
- Questions or comments?
-
Package/Label Principal Display Panel
CVS™
12 HR
actual size
Maximum Strength
Mucus-D
Guaifenesin & Pseudoephedrine Hydrochloride
Extended-Release Tablets
1200 mg / 120 mg
Expectorant, Nasal Decongestant
Compare to Maximum Strength Mucinex® D active ingredients
Clears Nasal & Sinus Congestion
Thins & Loosens Mucus
Immediate & Extended Release
Relieves Nasal & Chest Congestion
24 EXTENDED-RELEASE TABLETS
-
INGREDIENTS AND APPEARANCE
MUCUS D
guaifenesin, pseudoephedrine hydrochloride tablet, multilayer, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-345 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 1200 mg PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) FD&C YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D) Product Characteristics Color ORANGE Score no score Shape OVAL Size 22mm Flavor Imprint Code L12 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-345-62 4 in 1 CARTON 04/04/2025 1 6 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA214407 04/04/2025 Labeler - CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED (062312574)

