Overview
Rumex crispus whole 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 |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Nutritional Specialties, Inc. | 83027-0052 | ORAL | 6 [hp_X] in 1 mL | 5/15/2025 | |
| Newton Laboratories, Inc. | 55714-1736 | ORAL | 15 [hp_X] in 1 g | 5/7/2025 | |
| Newton Laboratories, Inc. | 55714-1536 | ORAL | 15 [hp_X] in 1 mL | 5/7/2025 |
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 |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| RUMEX GOUTTE 1DH-30CH | boiron laboratoires | 00670081 | Drops - Oral | 1 DH / DH | 12/31/1987 |
| RUMEX CRISPUS | seroyal international inc. | 02233198 | Tablet
,
Drops
,
Globules
,
Pellet
,
Granules
,
Liquid - Oral | 1 X | 4/6/1998 |
| RUMEX CRISPUS GRANULE(1CH-30CH) | homeocan inc. | 01949764 | Tablet - Oral | 1 CH / TAB | 12/31/1991 |
| RUMEX CRISPUS GRANULE 1DH-30CH | homeocan inc. | 01917870 | Tablet - Oral | 1 DH / TAB | 12/31/1992 |
| RUMEX-INJEEL FORTE LIQ (4D,8D,12D,30D,200D/1.1ML) | 02071851 | Liquid - Oral | 4 D / 1.1 ML | 12/31/1994 | |
| SCROPLEX | bio active canada ltd. | 02233682 | Liquid - Oral | 1 X | 5/26/1998 |
| THROAT | botanical laboratories inc. | 02233409 | Tablet - Oral | 6 X | 4/15/1998 |
| BR-NIX HP | terra botanica products ltd. | 02233302 | Liquid - Oral | 30 X | 5/25/1998 |
| BRON HP | bio active canada ltd. | 02233570 | Liquid - Oral | 30 X | 5/26/1998 |
| RUMEX GLOBULE 1DH-30CH | boiron laboratoires | 00683264 | Tablet - Oral | 1 DH / DH | 12/31/1986 |
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. | |||||
Help Us Improve
Your feedback helps us provide better drug information and insights.