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up and up fiber therapy by Target Corporation.

Dosage form: tablet
Ingredients: CALCIUM POLYCARBOPHIL 625mg
Labeler: Target Corporation.
NDC Code: 11673-620

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

up and up fiber therapy

Active ingredient (in each caplet)

Calcium polycarbophil 625 mg equivalent to 500 mg polycarbophil

Purpose

Bulk-forming laxative

Uses
relieves occasional constipation to help restore and maintain regularity
this product generally produces bowel movement in 12 to 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 your 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

Ask your doctor or pharmacist before use if

you are 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
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 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.

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
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 dose
 
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
each caplet contains: calcium 125 mg
do not use if printed seal under cap is torn or missing
store at 20-25°C (68-77°F)
protect contents from moisture

Inactive ingredients

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

Questions?

Call 1-800-910-6874

Principal Display Panel

NDC 11673-620-90

Compare to active ingredient in Fibercon® *

fiber therapy

calcium polycarbophil ,625 mg

bulk-forming laxative

helps relieve constipation and restore regularity

gentle enough to use every day

140 CAPLETS

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

245 05 0555 R01 ID295403

Dist.by Target Corp., Mpls., MN 55403

©2015 Target Brands, Inc.

Shop Target.com

UP AND UP FIBER THERAPY 
calcium polycarbophil tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-620
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM POLYCARBOPHIL (POLYCARBOPHIL) CALCIUM POLYCARBOPHIL625 mg
Inactive Ingredients
Ingredient NameStrength
CALCIUM CARBONATE 
CARAMEL 
CROSPOVIDONE 
HYPROMELLOSE 2208 (100 MPA.S) 
MAGNESIUM STEARATE 
MALTODEXTRIN 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOL 800 
SILICON DIOXIDE 
SODIUM LAURYL SULFATE 
Product Characteristics
ColorBROWN (light) Scoreno score
ShapeCAPSULE (caplet) Size19mm
FlavorImprint CodeRP120
Contains    
Packaging
#Item CodePackage Description
1NDC:11673-620-90140 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33410/14/2015
Labeler - Target Corporation. (006961700)

Revised: 12/2017
 
Target Corporation.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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