Label: FIBER THERAPY- methylcellulose powder, for solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 24, 2024

If you are a consumer or patient please visit this version.

  • Active ingredient (in each 19g adult dose/ rounded tablespoon)

    Methylcellulose 2g (a non-allergenic fiber)

  • Purpose

    Bulk-forming fiber laxative

  • Uses

    relieves constipation (irregularity)
    helps to restore and maintain regularity
    for treating bowel disorders when recommended by a doctor
    generally provide effect in 12-72 hours
  • Warnings

    CHOKING: taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking. Do not take this product if you have difficulty in swallowing. If you experience chest pain, vomiting, or difficulty in swallowing or breathing after taking this product, seek immediate medical attention.

    Ask a doctor before use if you have

    abdominal pain, nausea or vomiting
    a sudden change in bowel habits that persists over a period of 2 weeks
    sensitivity to any of the ingredients

    Stop use and ask a doctor if

    you have rectal bleeding
    you fail to have a bowl movement after use.
    These could be signs of a serious condition.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

    When using this product

    do not exceed recommended maximum daily dose unless directed by a doctor
    do not use laxative products for a period longer than one week unless directed by a doctor 
  • Directions

    MIX THIS PRODUCT (CHILD OR ADULT DOSE) WITH AT LEAST 8 OUNCES (A FULL GLASS) OF WATER OR OTHER FLUID. TAKING THIS PRODUCT WITHOUT ENOUGH LIQUID MAY CAUSE CHOKING. SEE CHOKING WARNING
    use product at the first sign of constipation or irregularity
    put one dose in a full glass of cold water
    stir briskly and drink promptly
    drinking another glass of water is helpful

    Age

    Dose

    adults & children above 12 years of age and over

    one rounded tablespoon. (19 g) in 8 ounces of water fluid up to 3 times daily at the first sign of constipation or irregularity

    children 6 - 12 years of age

    half the adult dose in 8 ounces of water once daily.

    children under 6 years of age

    ask a doctor

  • Other information

    each adult dose contains approximately
    3 mg of sodium
    105 mg potassium
    contributes 60 calories from sucrose and sorbitol
    store at room temperature
    protect contents from humidity
    keep tightly closed

     TAMPER EVIDENT: DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING

  • Inactive ingredients

    citric acid, FD&C yellow 6 aluminum lake, maltodextrin, flavor (natural and artificial), potassium citrate, silica, sucrose,

  • Questions or comments?

    1-800-616-2471

    *This product is not manufactured or distributed by GlaxoSmithKline the distributor of CITRUCEL®

    Distributed by:

    MAJOR® PHARMACEUTICALS

    17177 N Laurel Park Drive, Suite 233

    Relabeled By: Preferred Pharmaceuticals Inc.

    Livonia, MI 48152, USA

    Relabeled By: Preferred Pharmaceuticals Inc.

    DIRECTIONS FOR USE

    Image of pouring water into glass

    1. Fill glass with at least 8 ounces of cold water.

    Image of stirring water after adding Citrucel

    2. Add the adult or child dose listed in the directions. 3. Stir briskly until dissolved and drink promptly. Drinking an additional glass of water is helpful.

  • Principal Display Panel

    NDC 68788-7995-4

    Compare to the Active Ingredient in CITRUCEL®*

    FIBER THERAPY

    Methylcellulose

    Easy to Mix No Gritty Texture

    100% Soluble Fiber for Controlled Regularity

    ORANGE FLAVOR

    NET WT 16 OZ (454 GRAMS)

    Fiber Therapy Orange Flavored
  • INGREDIENTS AND APPEARANCE
    FIBER THERAPY 
    methylcellulose powder, for solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68788-7995(NDC:0904-5675)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYLCELLULOSE (4000 MPA.S) (UNII: MRJ667KA5E) (METHYLCELLULOSE (4000 MPA.S) - UNII:MRJ667KA5E) METHYLCELLULOSE (4000 MPA.S)2 g  in 19 g
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorORANGEScore    
    ShapeSize
    FlavorORANGEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68788-7995-4454 g in 1 BOTTLE; Type 0: Not a Combination Product08/09/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug33408/09/2021
    Labeler - Preferred Pharmaceuticals Inc. (791119022)
    Registrant - Preferred Pharmaceuticals Inc. (791119022)
    Establishment
    NameAddressID/FEIBusiness Operations
    Preferred Pharmaceuticals Inc.791119022RELABEL(68788-7995)