Home > Pill Identifier > Mucinex D Maximum Strength (guaifenesin 1200 MG / pseudoephedrine hydrochloride 120 MG) 12 HR Extended Release Tablet

Pill Identifier Information of Mucinex D Maximum Strength (guaifenesin 1200 MG / pseudoephedrine hydrochloride 120 MG) 12 HR Extended Release Tablet

Drug Information

Mucinex D Maximum Strength (guaifenesin 1200 MG / pseudoephedrine hydrochloride 120 MG) 12 HR Extended Release Tablet

Imprint: Mucinex;1200
Shape: C48345
Color: C48331;C48325
Ingredients: Guaifenesin; Pseudoephedrine
Size: 22.00
Score: 1
Rxtty: SY
Author: Reckitt Benckiser LLC
Inactive Ingredients: carbomer homopolymer type B (allyl pentaerythritol crosslinked) / FD&C yellow NO. 6 / aluminum oxide / hypromelloses / magnesium stearate / cellulose, microcrystalline>

Complete Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredients (in each extended-release tablet) Purposes
    Guaifenesin 1200 mg Expectorant
    Pseudoephedrine HCl 120 mg Nasal Decongestant

    Active ingredients (in each extended-release tablet)Purposes
    Guaifenesin 1200 mgExpectorant
    Pseudoephedrine HCl 120 mgNasal 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 useif 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.

  • Directions

  • Other information

  • Inactive ingredients

    carbomer homopolymer type B; FD&C yellow no. 6 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF

  • Questions?

    1-866-MUCINEX (1-866-682-4639)

  • SPL UNCLASSIFIED SECTION

    Dist. by: RB Health (US)
    Parsippany, NJ 07054-0224

    Made in England

  • PRINCIPAL DISPLAY PANEL - 24 Tablet Blister Pack Carton

    MAXIMUM STRENGTH

    NDC 63824-041-24

    Mucinex®D
    1200 mg guaifenesin & 120 mg pseudoephedrine HCl
    extended-release bi-layer tablets

    EXPECTORANT
    & NASAL DECONGESTANT

    12
    HOUR ®

    • Clears Nasal/Sinus Congestion
    • Thins and Loosens Mucus
    • Immediate and Extended Release

    24
    EXTENDED-RELEASE TABLETS

    Label

    label 3

  • INGREDIENTS AND APPEARANCE
    MUCINEX D  MAXIMUM STRENGTH
    guaifenesin and pseudoephedrine hydrochloride tablet, extended release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-041
    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)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    Product Characteristics
    Colororange, whiteScoreno score
    ShapeOVALSize22mm
    FlavorImprint Code Mucinex;1200
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-041-242 in 1 CARTON06/26/2012
    112 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:63824-041-7124 in 1 CARTON06/26/201207/10/2017
    21 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:63824-041-363 in 1 CARTON06/26/201209/12/2017
    312 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:63824-041-121 in 1 CARTON01/01/202012/31/2022
    412 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02158506/26/2012
    Labeler - Reckitt Benckiser LLC (094405024)