DRX CHOICE FIBER THERAPY- methylcellulose powder, for solution

DRx Choice Fiber Therapy by

Drug Labeling and Warnings

DRx Choice Fiber Therapy by is a Otc medication manufactured, distributed, or labeled by RARITAN PHARMACEUTICALS INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each rounded tablespoon)

Methylcellulose (a non-allergenic fiber) 2g

Purpose

Bulk-forming fiber laxative

Uses

• ▪ relieves occasional constipation (irregularity)
• ▪ generally produces a bowel movement 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

• ▪ a sudden change in bowel habits that persists for two weeks
• ▪ abdominal pain, nausea or vomiting

Stop use and ask a doctor if

• ▪ constipation lasts more than 7 days
• ▪ you have rectal bleeding

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.

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 12 years of age and over:

  start with 1 rounded tablespoon. Increase as needed, 1 rounded tablespoon at a time, up to 3 times per day.

• children 6 - 11 years of age:

  start with 2 level teaspoons. Increase as needed, 2 level teaspoons at a time, up to 3 times per day.

• children under 6 years of age:

  consult a physician

Other information

• each rounded tablespoon contains: calcium 85mg and potassium 125mg
• each rounded tablespoon contributes 27 calories from maltodextrin
• store at room temperature
• protect contents from humidity
• keep tightly closed

Inactive ingredients

Anhydrous citric acid, FD&C yellow #6 lake, flavor, maltodextrin, potassium citrate, silica, sucralose, tricalcium phosphate,

Questions or comments?

1-866-467-2748

Principal Display Panel

DRx Choice®

Compare to the Active Ingredient in Citrucel® Powder*

NDC: 68163-517-16

Sugar free

Soluble fiber therapy

Methylcellulose Fiber Therapy for Irregularity

• Gentle and clinically proven effective**
• Gives you additional fiber to help relieve occasional constipation

Fiber for irregularity that won’t cause excess gas***

Orange Flavor

Naturally & Artificially Flavored

NET WT 16.9 OZ (479g)

Directions for use:

• 1. Fill glass with at least 8 oz. of cold water.
• 2. Measure rounded tablespoon of product (one dose) and stir product into water. Stir briskly and drink promptly.

**When Used As Directed.

***Based On Laboratory Testing. Individual Results may Vary

TAMPER EVIDENT: DO NOT USE PRINTED INNER SEAL IS BROKEN OR MISSING

GLUTEN FREE

*This product is not manufactured or distributed by GSK Consumer Healthcare, the distributor of Citrucel® Powder.

Manufactured By:

Raritan Pharmaceuticals

8 Joana Court,

East Brunswick, NJ 08816

INGREDIENTS AND APPEARANCE

DRX CHOICE FIBER THERAPY 
methylcellulose powder, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68163-517
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYLCELLULOSE (4000 MPA.S) (UNII: MRJ667KA5E) (METHYLCELLULOSE (4000 MPA.S) - UNII:MRJ667KA5E)	METHYLCELLULOSE (4000 MPA.S)	2 g  in 10.2 g

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
POTASSIUM CITRATE (UNII: EE90ONI6FF)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SUCRALOSE (UNII: 96K6UQ3ZD4)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)

Product Characteristics
Color	ORANGE	Score
Shape		Size
Flavor	ORANGE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68163-517-16	479 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/18/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M007	07/18/2022

Labeler - RARITAN PHARMACEUTICALS INC (127602287)