Fiber Laxative by Geri-Care Pharmaceutical Corp gc449

Fiber Laxative by

Drug Labeling and Warnings

Fiber Laxative by is a Otc medication manufactured, distributed, or labeled by Geri-Care Pharmaceutical Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FIBER LAXATIVE- calcium polycarbophil tablet 
Geri-Care Pharmaceutical Corp

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.

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gc449

Active ingredient (in each caplet)

Calcium Polycarbophil 625 mg

(equivalent to 500 mg polycarbophil)

Purpose

Bulk-forming laxative

Uses

  • relieves occasional constipation
  • promotes regularity
  • this product generally produces a 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.


Do not use
for more than 1 week unless directed by a doctor

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.

Ask a doctor or pharmacist before use if you are

taking any other drug

all laxatives may affect how other drugs work.

Stop use and ask a doctor if

you have rectal bleeding

you have no bowel movement within 3 days

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.

Directions

do not exceed recommended dose

take each dose with at least 8 ounces (a full glass) of fluid; taking this product without enough liquid may cause choking; see choking warning

do not take this product within 2 hours before or after taking any other drug

adults and children 12
years of age and older
Starting dose: 2 caplets once a day
Maximum dose: 2 caplets four times a day
Starting dose: 2 caplets once a day
Maximum dose: 2 caplets four times a day
consult a doctor

Other information

each caplet contains: calcium 125 mg

store at controlled room temperature, 68°F-77°F (20°C-25°C)

protect contents from moisture

for institutional use only

Tamper Evident: Do not use if imprinted seal under cap is missing or broken.

Inactive ingredients

caramel color, croscarmellose sodium, hypromellose, microcrystalline cellulose, PEG, silica, talc

Package Label

GERICARE

NDC: 57896-449-09
Fiber Laxative
Calcium Polycarbophil

Relieves Constipation

Promotes Regularity

90 Caplets

625 mg Each

Compare to active ingredient

in FiberCon®*

Fiber Laxative label

FIBER LAXATIVE 
calcium polycarbophil tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 57896-449
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM POLYCARBOPHIL (UNII: 8F049NKY49) (POLYCARBOPHIL - UNII:W25LM17A4W) CALCIUM POLYCARBOPHIL625 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TALC (UNII: 7SEV7J4R1U)  
CARAMEL (UNII: T9D99G2B1R)  
Product Characteristics
Colorbrown (Off white with dark brown specks) Scoreno score
ShapeOVAL (Caplet) Size20mm
FlavorImprint Code AZ221
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 57896-449-0990 in 1 BOTTLE; Type 0: Not a Combination Product01/01/200412/30/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33401/01/200412/30/2019
Labeler - Geri-Care Pharmaceutical Corp (611196254)
Registrant - Geri-Care Pharmaceutical Corp (611196254)

Revised: 12/2019