Home > Pill Identifier > Mucinex 1200 MG 12 HR Extended Release Tablet

Pill Identifier Information of Mucinex 1200 MG 12 HR Extended Release Tablet

Drug Information

Mucinex 1200 MG 12 HR Extended Release Tablet

Imprint: Mucinex;1200
Shape: C48345
Color: C48325
Ingredients: Guaifenesin
Size: 22.00
Score: 1
Rxtty: SY
Author: Reckitt Benckiser LLC
Inactive Ingredients: Carbomer Homopolymer Type B (Allyl Pentaerythritol Crosslinked) / FD&C blue no. 1 / aluminum oxide / hypromelloses / magnesium stearate / cellulose, microcrystalline>

Complete Information

  • Warnings

    Do not use
    • for children under 12 years of age

    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)

    • 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 right away.

  • 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 the timing of meals
    • adults and children 12 years of age and over: 1 extended-release tablet every 12 hours. Do not exceed 2 extended-release tablets in 24 hours.
    • children under 12 years of age: do not use
  • Other information

  • Inactive ingredients

    carbomer homopolymer type B; FD&C blue no. 1 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 - 14 Tablet Blister Pack Carton

    NDC 63824-023-35

    MAXIMUM STRENGTH

    Mucinex®
    1200 mg guaifenesin
    extended-release tablets

    EXPECTORANT

    12
    HOUR ®

    • Relieves Chest Congestion
    • Thins and Loosens Mucus
    • Immediate and Extended Release

    EXTENDED-RELEASE TABLETS

    full carton label

  • INGREDIENTS AND APPEARANCE
    MUCINEX  MAXIMUM STRENGTH
    guaifenesin tablet, extended release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-023
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN1200 mg
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    Product Characteristics
    Colorwhite (blue and white) Scoreno score
    ShapeOVALSize22mm
    FlavorImprint Code Mucinex;1200
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-023-071 in 1 CARTON06/11/2015
    17 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:63824-023-351 in 1 CARTON06/26/2012
    214 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:63824-023-362 in 1 CARTON06/26/2012
    314 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:63824-023-484 in 1 CARTON06/26/2012
    412 in 1 BLISTER PACK; Type 0: Not a Combination Product
    5NDC:63824-023-463 in 1 CARTON06/26/2012
    514 in 1 BLISTER PACK; Type 0: Not a Combination Product
    6NDC:63824-023-182 in 1 CARTON06/26/201206/15/2022
    69 in 1 BLISTER PACK; Type 0: Not a Combination Product
    7NDC:63824-023-021 in 1 CARTON07/01/2021
    71 in 1 POUCH; Type 0: Not a Combination Product
    8NDC:63824-023-564 in 1 CARTON07/01/2021
    814 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02128206/26/2012
    Labeler - Reckitt Benckiser LLC (094405024)