Overview
Spearmint allergenic extract is used in allergenic testing.
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 |
---|---|---|---|---|---|
Nelco Laboratories, Inc. | 36987-1742 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/9/2009 | |
Allergy Laboratories, Inc. | 54575-459 | PERCUTANEOUS, SUBCUTANEOUS | 1 g in 20 mL | 3/15/2011 | |
Nelco Laboratories, Inc. | 36987-1743 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/9/2009 | |
Antigen Laboratories, Inc. | 49288-0304 | SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 11/17/2009 | |
Nelco Laboratories, Inc. | 36987-1745 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/9/2009 | |
Nelco Laboratories, Inc. | 36987-1744 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/9/2009 |
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 |
---|---|---|---|---|---|
Swisse Ultivite Women's High Potency Multivitamin | 369430 | Medicine | A | 6/16/2021 | |
Swisse Ultivite Men's 50+ Multivitamin | 380937 | Medicine | A | 12/16/2021 | |
ATHELITE LAVA ICE JOINT & MUSCLE PAIN RELIEF SPRAY | 428839 | Medicine | A | 11/28/2023 | |
Swisse Ultivite Vegan Women's Multivitamin | 385412 | Medicine | A | 3/10/2022 | |
NZ Swisse Women's Ultivite 50+ | 324281 | Medicine | A | 9/30/2019 | |
Swisse Ultivite Men's 65+ Multivitamin | 387191 | Medicine | A | 4/19/2022 | |
HKSG Swisse Ultivite Men's 50+ Multivitamin | 323148 | Medicine | A | 9/13/2019 | |
ATHELITE LAVA ICE JOINT & MUSCLE PAIN RELIEF & RECOVERY CREAM | 428837 | Medicine | A | 11/28/2023 | |
MALE UP&GO | 477152 | Medicine | A | 1/30/2025 | |
Clear Nausea Relief | 489146 | Medicine | A | 5/19/2025 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
STOMACH TEA | 3 way herbs ltd. | 00582751 | Tea (Herbal) - Oral | 8 % | 12/31/1983 |
FLORA HERBTEA SPEARMINT LEAVES | flora manufacturing and distributing ltd. | 00324035 | Tea (Herbal) - Oral | null NIL / NIL | 12/31/1975 |
FLORADIX MULTIZYME HERBAL TAB | salus-haus | 00307661 | Tablet - Oral | 15 MG | 12/31/1974 |
FLORADIX MULTIZYME HERBAL TAB | salus-haus | 00307661 | Tablet - Oral | 30 MG | 12/31/1974 |
PHYTOCALM | santé naturelle (ag) ltée | 00485179 | Tea (Herbal) - Oral | 220 MG / G | 12/31/1981 |
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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