CDMA Fiber Therapy

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION
Effective date
2025-12-03
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:19:22

Label at a glance#

ProductCDMA Fiber Therapy
Active ingredientMETHYLCELLULOSE (4000 MPA.S)
Label structure7 sections

Indications and uses

helps restore and maintain regularity relieves constipation (irregularity) for constipation associated with other bowel disorders like IBS when recommended by a doctor. generally produces a bowel movement in 12 -72 hours. 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....

Dosage and administration

Take 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. Age Dose Maximum Dose adults & children 12 years of age and over start with 2 caplets. Increase as needed up to 6 times per day. Do not exceed 12 caplets per day Children 6-11 years of age Start with 1 caplet. Increase as needed up ...

Label contents#

Full prescribing information#

Active ingredient (in each caplet)

OTC - ACTIVE INGREDIENT SECTION

Methylcellulose 500mg

Purpose

OTC - PURPOSE SECTION

Bulk-forming fiber laxative (a non-allergenic fiber)

Uses

INDICATIONS & USAGE SECTION

  • helps restore and maintain regularity
  • relieves constipation (irregularity)
  • for constipation associated with other bowel disorders like IBS when recommended by a doctor.
  • generally produces a bowel movement in 12 -72 hours.

Warnings

WARNINGS SECTION

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

OTC - ASK DOCTOR SECTION

  • a sudden change in bowel habits that persists over a period of two weeks
  • abdominal pain, nausea or vomiting
Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Constipation lasts more than 7 days
  • you have rectal bleeding
  • These could be signs of a serious condition.
Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Take 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.

Age

Dose

Maximum Dose

adults & children 12 years of age and over

start with 2 caplets. Increase as needed up to 6 times per day.

Do not exceed 12 caplets per day

Children 6-11 years of age

Start with 1 caplet. Increase as needed up to 6 times per day

Do not exceed 6 caplets per day

children under 6 years of age

Consult a physician

Consult a physician

Other information

SPL UNCLASSIFIED SECTION

  • each caplet contains: appx. 18 mg of calcium
  • store at below 77° F (25°C)
  • protect contents from humidity
  • keep tightly closed

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

adipic acid, calcium carbonate, crospovidone, FD&C yellow no. 6 aluminum lake, magnesium stearate, maltodextrin, microcrystalline cellulose, polysorbate 80, silica.

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

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Quality Choice ®

NDC# 63868-166-10

Compare to Citrucel ®Caplets Active Ingredients*

Fiber Therapy

Fiber Therapy for Regularity

Methylcellulose

  • 100% non-allergenic
  • Gentle and Gluten-Free
  • 100 CAPLETS

100% QC SATISFACTION GURANTEED

Distributed by C.D.M.A., Inc. ©

43157 W. Nine Mile

Novi, MI 48376-0995

www.qualitychoice.com

Questions: 248-449-9300

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

QC(CDMA) Fiber Therapy for Regularity 100 Caplets
QC(CDMA) Fiber Therapy for Regularity 100 Caplets

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198750methylcellulose 500 MG Oral TabletPSN6
198750methylcellulose 500 MG Oral TabletSCD6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63868-166-10CDMA Fiber Therapy100 in 1 BOTTLETABLET1006

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63868-166-10EA - Each63868-166de56e60f-3806-453f-aaa7-5ad05d074d5912022-08-04

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63868-16663868-166-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CDMA Fiber TherapyMETHYLCELLULOSECHAIN DRUG MARKETING ASSOCIATION62bbcaf2-1d0c-485f-9159-685700aa34182025-12-03WarningsExact identifier
ndc (package): 63868-166-10
ndc (product): 63868-166
ndc11 (package): 63868016610
spl id: 45098ea5-f856-fd5c-e063-6394a90a2edc
spl set id: 62bbcaf2-1d0c-485f-9159-685700aa3418

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.