Overview
Rhubarb allergenic extract is used in allergenic testing.
Indication
No indication information available.
Associated Conditions
- Constipation
- Decreased appetite
- Gingivitis
- Occasional Constipation
- Oropharyngitis
- Pain, Orofacial
- Gum pain
- Swelling of the gums
- Swelling of the mouth
- Ulceration of the mouth
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2021/08/04 | Not Applicable | Not yet recruiting | Fifth Affiliated Hospital, Sun Yat-Sen University | ||
2008/12/30 | Phase 2 | UNKNOWN | |||
2008/11/11 | Phase 2 | UNKNOWN |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Allergy Laboratories, Inc. | 54575-451 | PERCUTANEOUS, SUBCUTANEOUS | 1 g in 20 mL | 3/15/2011 | |
| Nelco Laboratories, Inc. | 36987-1505 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/9/2009 | |
| Nelco Laboratories, Inc. | 36987-1504 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/9/2009 | |
| Nelco Laboratories, Inc. | 36987-1503 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/9/2009 | |
| Nelco Laboratories, Inc. | 36987-1502 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/9/2009 | |
| Laboratoires Boiron | 0220-9054 | ORAL | 5 [hp_C] in 1 1 | 5/27/2025 | |
| PureTek Corporation | 59088-156 | ORAL | 4 mg in 1 1 | 12/18/2023 |
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 |
|---|---|---|---|---|---|
| SANKAIJO TABLET | SIN03486P | TABLET, FILM COATED | 25 mg | 6/24/1989 |
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 |
|---|---|---|---|---|---|
| FIX No.2 Control | 431371 | Medicine | A | 12/20/2023 | |
| Hilde Hemmes' Herbals Swedish Bitters Capsules | 82846 | Medicine | A | 5/21/2002 | |
| EMO)DIN | 199243 | Medicine | A | 7/10/2012 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| CONSOLIN | dolisos laboratoires s.a. | 02242708 | Syrup - Oral | 3 CH / 25 ML | 3/9/2001 |
| RHEUM-INJEEL FORTE LIQ (4D,8D,12D,30D,200D/1.1ML) | 02071940 | Liquid - Oral | 4 D / 1.1 ML | 12/31/1994 | |
| MULTILAX 2 TAB | nature's way of canada ltd. | 00627984 | Tablet - Oral | 40 MG / TAB | 12/31/1984 |
| HERBAL LAXATIVE FORMULA | wn pharmaceuticals ltd. | 02247019 | Tablet - Oral | 4 MG | 2/25/2004 |
| VITA-LAX | bio vita | 00472743 | Tablet - Oral | 8 MG | 12/31/1991 |
| NEO-LAX TAB | golden neo-life international ltd. | 00661635 | Tablet - Oral | 15 MG / TAB | 12/31/1986 |
| HERBAL LAX | creative nutrition canada corp. | 00614742 | Tablet - Oral | 8 MG / TAB | 12/31/1984 |
| NOVILAX TAB | le groupe prodeal ltee | 00774596 | Tablet - Oral | 8 MG / TAB | 12/31/1988 |
| HERBAL LAXATIVE TAB | nutrition for life international | 02057646 | Tablet - Oral | 8 MG / TAB | 11/27/1996 |
| HERBAL LAXATIVE FORMULA CAPLET | health-wise nutrition inc. | 02023547 | Tablet - Oral | 10 MG | 12/31/1995 |
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.