FIBER THERAPY- methylcellulose powder, for solution 
Major Pharmaceuticals

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Drug Facts

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

Children under 6 years of age

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

ask a doctor

Other information

Each adult dose contains approximately
3mg of sodium
105mg 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?

call toll-free 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

Livonia, MI 48152, USA

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.

TAMPER EVIDENT PACKAGE

Do not use if printed seal under cap is torn or missing.

Principal Display Panel

NDC 0904-5675-16

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
FIBER THERAPY 
methylcellulose powder, for solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)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)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
RIBOFLAVIN (UNII: TLM2976OFR)  
SUCROSE (UNII: C151H8M554)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SORBITOL (UNII: 506T60A25R)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorORANGEScore    
ShapeSize
FlavorORANGEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0904-5675-16454 g in 1 BOTTLE; Type 0: Not a Combination Product04/18/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00704/18/2008
Labeler - Major Pharmaceuticals (191427277)

Revised: 10/2023
Document Id: 30635d66-a6f0-4b15-b007-526f56c1afd0
Set id: 5dddab8d-0041-4486-9ed9-1dbd13575b47
Version: 8
Effective Time: 20231027
 
Major Pharmaceuticals