MedPath

Glycyrrhiza glabra

Generic Name
Glycyrrhiza glabra
Drug Type
Biotech
CAS Number
84775-66-6
Unique Ingredient Identifier
2788Z9758H

Overview

Glycyrrhiza glabra is a plant/plant extract used in some OTC (over-the-counter) products. It is not an approved drug.

Indication

No indication information available.

Associated Conditions

  • Anxiety
  • Mucus Retention
  • Nausea

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
BioActive Nutritional, Inc.
43857-0057
ORAL
1 [hp_X] in 1 mL
5/20/2025
Deseret Biologicals, Inc.
43742-1312
ORAL
3 [hp_X] in 1 mL
5/27/2025
Dr. Donna Restivo DC
62185-0062
ORAL
3 [hp_X] in 1 mL
5/23/2025

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
AFRICAN SEA-COCONUT COUGH MIXTURE
SIN03619P
SOLUTION
0.112ml/5ml
7/15/1989
NEW TONIN TROCHE L
SIN04537P
LOZENGE
125 mg
5/21/1990

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.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
Swisse Ultiboost Sleep
327845
Medicine
A
12/17/2019
Cellula-T oral powder jar
43995
Hong Sp & Hs
Medicine
A
4/13/1993
Kiwiherb Echinature
335157
Phytomed Australia Pty Ltd
Medicine
A
4/25/2020
2210 (Kaiser Pharmaceutical) Gui Zhi Tang (Cinnamon Combination)
218806
Medicine
A
12/24/2013
3650 (Kaiser Pharmaceutical) Bu Zhong Yi Qi Tang (Ginseng & Astragalus Combination)
229406
Medicine
A
10/15/2014
Zinc Repair Formula
356881
Medicine
A
3/17/2021
Stress Forte
373634
RN Labs Pty Ltd
Medicine
A
8/27/2021
Adrenal Adapt
444375
Medicine
A
3/25/2024
METAGENICS G-TOX EXPRESS
371950
Medicine
A
8/2/2021
Gut Calm + Restore
444372
Medicine
A
3/25/2024

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
CHEST AND COUGH HERB TEA NO 2 DR SCHIEFFER
dr nachf dr. nachf grunitz chemische erzeugnisse
00218278
Tea (Herbal) - Oral
20 %
12/31/1951
ADAPTAGEN
bio active canada ltd.
02233546
Liquid - Oral
3 X
5/26/1998
STOMACH TEA
3 way herbs ltd.
00582751
Tea (Herbal) - Oral
8 %
12/31/1983
THC COMPLEX #71
total health centre
02236390
Drops - Oral
1 X
3/29/1998
THUNAS NATURAL AID TAB
thuna herbal remedies ltd.
00386219
Tablet - Oral
83.2 MG
12/31/1979
ARTHRITIS PAIN RELIEF - CAP
jamieson laboratories ltd
02230232
Capsule - Oral
25.62 MG / CAP
7/17/1997
LIQUISAN SYR FOR COUGH NO2
a g kunzle krauterpfarrer ag
00125520
Syrup - Oral
3 %
12/31/1951
LIVER AND KIDNEY TEA THUNAS
thuna herbal remedies ltd.
00190446
Tea (Herbal) - Oral
2.27 G / 30 G
6/11/1980
HERBAL LAXATIVE FORMULA
wn pharmaceuticals ltd.
02247019
Tablet - Oral
40 MG
2/25/2004
VITALP PLUS EUCALYPTUS
domaco dr med aufdermaur ag
02237554
Lozenge - Oral
81.18 MG / LOZ
N/A

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
IBEROGAST GOTAS ORALES EN SOLUCION
Bayer Hispania S.L.
75509
GOTAS ORALES EN SOLUCIÓN
Sin Receta
Commercialized
IBEROGAST ELEMENTAL GOTAS ORALES EN SOLUCION
Bayer Hispania S.L.
88986
GOTAS ORALES EN SOLUCIÓN
Sin Receta
Not Commercialized
IBEROGAST GOTAS ORALES EN SOLUCION
Bayer Bulgaria Eood
8900
GOTAS ORALES EN SOLUCIÓN
Sin Receta
Commercialized

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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