MedPath

Urtica dioica pollen

Generic Name
Urtica dioica pollen
Drug Type
Biotech
Unique Ingredient Identifier
DNB59M1NVU

Overview

Urtica dioica pollen is the pollen of the Urtica dioica plant. Urtica dioica pollen is mainly 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.
36987-3299
SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
12/4/2009
Antigen Laboratories, Inc.
49288-0853
SUBCUTANEOUS, INTRADERMAL
0.0004 g in 1 mL
5/11/2012
Antigen Laboratories, Inc.
49288-0793
SUBCUTANEOUS, INTRADERMAL
0.0016666 g in 1 mL
10/13/2010
Nelco Laboratories, Inc.
36987-3293
SUBCUTANEOUS, INTRADERMAL
10000 [PNU] in 1 mL
12/4/2009
Antigen Laboratories, Inc.
49288-0827
INTRADERMAL, SUBCUTANEOUS
0.0004 g in 1 mL
11/22/2011
Nelco Laboratories, Inc.
36987-3298
SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
12/4/2009
Antigen Laboratories, Inc.
49288-0330
SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
11/13/2009
Antigen Laboratories, Inc.
49288-0714
SUBCUTANEOUS, INTRADERMAL
0.00833 g in 1 mL
12/2/2009
Nelco Laboratories, Inc.
36987-3296
SUBCUTANEOUS, INTRADERMAL
20000 [PNU] in 1 mL
12/4/2009
Antigen Laboratories, Inc.
49288-0852
SUBCUTANEOUS, INTRADERMAL
0.002 g in 1 mL
5/11/2012

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
Blackmores Bio Iron (NZ)
143952
Medicine
A
8/29/2007
Total Prostate
301500
Medicine
A
4/3/2018
HKSG Swisse Kids Multi
321304
Medicine
A
8/5/2019
Herbal Vitality
314808
Lyndelen Pty Ltd T/A The Herbal Extract Co of Australia
Medicine
A
2/26/2019
Swisse Ultivite Children's Multivitamin
276713
Medicine
A
6/17/2016
WelleCo Australia The PMS Elixir
380270
Medicine
A
12/6/2021
Testorod
408550
Medicine
A
5/5/2023
ErectOMax
158271
Medicine
A
1/5/2009
Premium Prostate Care
352556
B Pure Australia Pty Ltd
Medicine
A
1/6/2021
VN Swisse Ultivite Children's Multivitamin
470154
Medicine
A
11/25/2024

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
JUNIPLEX I
bio active canada ltd.
02233640
Liquid - Oral
1 X
5/26/1998
URTICA DIOICA FEC D2 (D3) - LIQUID
weleda ag heilmittelbetriebe
02172232
Liquid - Oral
2 D / ML
4/9/1998
APIZELEN
bio active canada ltd.
02233553
Liquid - Oral
2 C
5/26/1998
POUR IT ON THICK
kootenay born botanicals
02232067
Syrup - Oral
1 X
5/25/1998
BAYBERRYPLEX
bio active canada ltd.
02233592
Liquid - Oral
1 X
5/26/1998
TUSNIX SYRUP
terra botanica products ltd.
02233376
Liquid - Oral
1 X
2/2/1998
TRIFOLOPLEX
bio active canada ltd.
02233689
Liquid - Oral
1 X
5/26/1998
ACALYPHA INDICA GRANULE (1DH-30DH)
homeocan inc.
01960849
Tablet - Oral
1 DH
12/31/1992
URTICA DIOICA DROPS
weleda ag heilmittelbetriebe
02232641
Drops - Oral
1 D
4/8/1998
ARTHRICIN
botanical laboratories inc.
02233396
Tablet - Oral
3 X
4/15/1998

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.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.