Quality Choice

Manufacturer
QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
Effective date
2025-07-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:06:45

Label at a glance#

ProductQuality Choice Fiber Caplets
Active ingredientCALCIUM POLYCARBOPHIL
Label structure9 sections

Dosage and administration

Take each dose of this product 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). This product works naturally so continued use for one to three days is normally required to provide full benefit. Dosage may vary according to diet, exercise, previous laxative use or severity of constipation. age Recommended Daily maximum...

Label contents#

Full prescribing information#

Drug Fats

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each caplet)

Calcium polycarbophil 625 mg equivalent to 500 mg polycarbophil

OTC - PURPOSE SECTION

Purpose

Bulk-forming laxative

U ses

INDICATIONS & USAGE SECTION

  • relieves occasional constipation to help restore and maintain regularity
  • this product generally produces bowel movement in 12 to 72 hours

WARNINGS SECTION

Choking Warning: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 your doctor before use if you have

OTC - ASK DOCTOR SECTION

  • abdominal pain, nausea, or vomiting
  • a sudden change in bowel habits that persists over a period of 2 weeks

Ask your doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking any other drug. Take this product 2 or more hours before or after other drugs. All laxatives may affect how other drugs work.

When using this product

OTC - WHEN USING SECTION

  • do not use for more than 7 days unless directed by a doctor
  • do not take more than 8 caplets in a 24 hour period unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

rectal bleeding occurs or if you fail to have a bowel movement after use of this or any other laxative. These could be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE 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 each dose of this product 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).
  • This product works naturally so continued use for one to three days is normally required to provide full benefit. Dosage may vary according to diet, exercise, previous laxative use or severity of constipation.

age

Recommended

Daily maximum

adults & children 12 years of age and over

2 caplets once a day

up to 4 times a day

children under 12 years

consult a physician

Other information

SPL UNCLASSIFIED SECTION

  • each caplet contains: calcium 125 mg
  • store at room temperature
  • protect contents from moisture

INACTIVE INGREDIENT SECTION

calcium carbonate, caramel, crospovidone, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, silicon dioxide, sodium lauryl sulfate.

Questions or Comments?

OTC - QUESTIONS SECTION

1-866-467-2748

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC# 83324-276-90

QUALITY CHOICE ®

*Compare to the Active ingredients in Fibercon ®

Fiber Caplets

Calcium Polycarbophil 625 mg

Bulk-Forming

Fiber Laxative

Won’t Cause Gas or Bloating As Effective as Fiber Powders

90 Caplets

100% QC SATISFACTION GURANTEED

Distributed by C.D.M.A., Inc.

Novi, MI 48375

www.qualitychoice.com

Questions: 800-935-2362

DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING

*This product is not manufactured or distributed by Pfizer Inc., owner of the registered trademark Fibercon® Caplets.

Package label for 90 Caplets

Quality Choice Fiber Caplets 90 Caplets
Quality Choice Fiber Caplets 90 Caplets

Package Label for 140 Caplets

SPL UNCLASSIFIED SECTION

Quality Choice Fiber Caplets 140 Caplets
Quality Choice Fiber Caplets 140 Caplets

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308934calcium polycarbophil 625 MG Oral TabletPSN2
308934calcium polycarbophil 625 MG Oral TabletSCD2
308934calcium polycarbophil 625 MG (as polycarbophil 500 MG) Oral TabletSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83324-276-14Quality ChoiceFiber Caplets140 in 1 BOTTLETABLET, FILM COATED1402
83324-276-90Quality ChoiceFiber Caplets90 in 1 BOTTLETABLET, FILM COATED902

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
83324-276-90EA - Each83324-276be312020-8940-4d5a-8298-3598bf2ed29712025-08-11

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83324-27683324-276-90, 83324-276-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
Quality Choice Fiber CapletsCALCIUM POLYCARBOPHILQUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)29dbc831-23c1-487d-902a-9404d9ebe8052025-07-09WarningsExact identifier
ndc (package): 83324-276-90
ndc (package): 83324-276-14
ndc (product): 83324-276
ndc11 (package): 83324027614
ndc11 (package): 83324027690
spl id: 39825b7a-6cae-ddd7-e063-6394a90a3972
spl set id: 29dbc831-23c1-487d-902a-9404d9ebe805

Reported adverse events (FAERS/openFDA)#

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