MedPath

Spearmint

Generic Name
Spearmint
Drug Type
Biotech
Unique Ingredient Identifier
J7I2T6IV1N

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.

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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