Overview
Milk thistle 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
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2016/07/25 | Phase 2 | Withdrawn | |||
2015/06/17 | Phase 2 | Completed | |||
2015/01/13 | Phase 2 | Completed | |||
2009/10/28 | Phase 2 | Completed | |||
2009/10/27 | Phase 2 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Newton Laboratories, Inc. | 55714-2596 | ORAL | 15 [hp_X] in 1 mL | 5/21/2025 | |
| Deseret Biologicals, Inc. | 43742-2263 | ORAL | 6 [hp_X] in 1 mL | 5/7/2025 | |
| Newton Laboratories, Inc. | 55714-4862 | ORAL | 15 [hp_X] in 1 mL | 5/21/2025 | |
| Bestmade Natural Products | 82969-2062 | ORAL | 200 [hp_C] in 200 [hp_C] | 1/30/2025 | |
| Deseret Biologicals, Inc. | 43742-2244 | ORAL | 6 [hp_X] in 1 mL | 5/27/2025 | |
| Bestmade Natural Products | 82969-2065 | ORAL | 30 [hp_C] in 30 [hp_C] | 1/30/2025 | |
| Bestmade Natural Products | 82969-2052 | ORAL | 100 [hp_C] in 100 [hp_C] | 1/23/2025 | |
| Newton Laboratories, Inc. | 55714-4838 | ORAL | 15 [hp_X] in 1 mL | 5/21/2025 | |
| Bestmade Natural Products | 82969-2058 | ORAL | 10 [hp_C] in 20 [hp_C] | 1/24/2025 | |
| Dr. Donna Restivo DC | 62185-0065 | 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 |
|---|---|---|---|---|---|
| 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. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| One A Day Adults Heart & Liver Capsules | 439795 | Medicine | A | 2/5/2024 | |
| MOM'S GARDEN® LIVER SUPPORT | 486006 | Medicine | A | 4/14/2025 | |
| PRINCESS LUNA® LIVER SUPPORT | 474885 | Medicine | A | 1/2/2025 | |
| PRINCESS LUNA® LIVER SUPPORT | 476605 | Medicine | A | 1/24/2025 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| BIOSTRATH NO 6 | bio-strath ag | 00661112 | Suspension - Oral | .225 ML / ML | 12/31/1989 |
| R7 DPS | dr reckeweg canada | 02089386 | Drops - Oral | 2 D / ML | 12/31/1994 |
| HEPEEL | 02229470 | Liquid - Oral | 1 D / 1.1 ML | 10/1/1996 | |
| CARDUUS MARIANUS | seroyal international inc. | 02233109 | Globules
,
Capsule
,
Liquid
,
Powder
,
Granules
,
Pellet
,
Tablet
,
Drops - Oral | 1 X | 4/6/1998 |
| CHELIDONIUM PLEX | seroyal international inc. | 02233115 | Granules
,
Pellet
,
Tablet
,
Syrup
,
Liquid
,
Drops - Oral | 1 X | 4/6/1998 |
| HEPTOX | bio active canada ltd. | 02233624 | Liquid - Oral | 12 X | 5/26/1998 |
| DANDI COMP | kootenay born botanicals | 02232052 | Liquid - Oral | 1 X | 5/15/1998 |
| MEDIPLEX 640 - LIQ | mediherb inc. | 02116901 | Liquid - Oral | 10 X / ML | 12/19/1996 |
| CHELIDONIUM COMPOSE DPS | homeocan inc. | 02098695 | Drops - Oral | 1 CH / ML | 12/31/1994 |
| CARDUUS MARIANUS | total health centre | 02236270 | Drops - Oral | 1 X | 4/1/1998 |
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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