MedPath

Plantago seed

Generic Name
Plantago seed
Brand Names
Konsyl, Metamucil, Reguloid
Drug Type
Biotech
CAS Number
8063-16-9
Unique Ingredient Identifier
9C60Y73166

Overview

Platango seeds refer to the seeds collected from various species of plantago trees. It is found in some laxatives for treating occasional constipation and restoring regularity in bowel movements. Its potential benefit in maintaining remission in ulcerative colitis has been studied . Regardless, this agent is most predominantly used as a gentle laxative agent in many parts of the world that is more commonly referred as psyllium or psyllium husk.

Indication

Indications include the treatment of patients needing a high fibre regime, perhaps for: (a) the relief of constipation, including constipation in pregnancy and the maintenance of regularity; (b) the management of bowel function in patients with colostomy, ileostomy, hemorrhoids, anal fissure, chronic diarrhea with diverticular disease, irritable bowel syndrome, and ulcerative colitis .

Associated Conditions

  • Bowel Motility
  • Constipation

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/10/15
Phase 2
Recruiting
Dr Bruno Chumpitazi, M.D.
2023/12/12
Phase 2
Not yet recruiting
2023/05/22
Phase 4
Completed
2018/09/13
Phase 4
Completed
West Side Institute for Science and Education
2016/08/16
Not Applicable
Completed
Amsterdam UMC, location VUmc
2014/05/22
Phase 2
Terminated
2014/05/13
Phase 4
Completed
Francesco Gabrielli
2010/12/02
Phase 4
Completed
2008/08/04
Phase 2
Completed
2005/09/16
Not Applicable
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Raritan Pharmaceuticals Inc
68163-571
ORAL
3.4 g in 12 g
4/8/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
MULTILAX 1 CAP
nature's way of canada ltd.
00629561
Capsule - Oral
378 MG / CAP
12/31/1984
HM-LAX CAP 435MG
nutrition professionals inc.
00643807
Capsule - Oral
435 MG / CAP
12/31/1988
FIBRE LAXATIVE EXTRA SMOOTH-PWR 3.4GM/12GM
vita health products inc
02157276
Powder - Oral
3.4 G / 12 G
12/31/1995
SSMO COMPLEX DPS
thompson's homeopathic supplies ltd.
00757381
Drops - Oral
3 X / X
12/31/1987
PSYLLIUM BLOND
laboratoire atlas inc
00050172
Seed - Oral
null NIL / NIL
12/31/1951
PRODIEM PLUS POWDER
rhone-poulenc rorer consumer inc.
01937626
Powder - Oral
542 MG / G
12/31/1993
PLANTAGO MAJOR GRANULE 1DH - 30CH
dolisos laboratoires s.a.
00699160
Tablet - Oral
1 DH / DH
12/31/1987
PLANTAGO MAJOR GOUTTE 4CH-30CH
dolisos laboratoires s.a.
00684260
Drops - Oral
1 CH / CH
12/31/1987
NAT.SOURCE FIBRE LAX.SM.TEX.-SUGAR FREE
stanley pharmaceuticals, a division of vita health products inc.
02067552
Powder - Oral
3.4 G / 5.8 G
12/31/1995
NATURAL SOURCE LAXATIVE PWR
novopharm limited
00551546
Powder - Oral
3 G / 6.2 G
12/31/1989

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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