MedPath

Rosemary

Generic Name
Rosemary
Drug Type
Biotech
Unique Ingredient Identifier
IJ67X351P9

Overview

Rosemary 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
Shantou Youjia E-Commerce Co., Ltd.
84067-150
CUTANEOUS
25 mg in 100 mg
3/11/2024

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
Lifetime Brain Q
297835
Medicine
A
12/20/2017
Herbal Vitality
314808
Lyndelen Pty Ltd T/A The Herbal Extract Co of Australia
Medicine
A
2/26/2019
Immune Health
235223
Medicine
A
3/19/2015
BIOGLAN MEN XPERT LUNG HEALTH WITH QUERCETIN
399450
Medicine
A
11/15/2022
Akaure Vibrant Mind
445602
Medicine
A
4/10/2024
GARLIC ALLIUM COMPLEX
407010
Medicine
A
3/29/2023
Breathe Easy
473413
The Breath of Life
Medicine
A
12/17/2024
PM Essentials
342492
Regulatory Services Australia
Medicine
A
8/27/2020
Brain Power Roll On
226545
Medicine
A
8/4/2014
NUTRIWAY DOUBLE X PHYTONUTRIENT SUPPLEMENT
339053
Medicine
A
7/7/2020

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
ROSMARINUS OFFICINALIS-INJEEL LIQ (8D,12D,30D,200D/1.1ML)
02071886
Liquid - Oral
8 D / 1.1 ML
12/31/1994
ROSMARINUS OFFICINALIS GOUTTE 4CH-30CH
dolisos laboratoires s.a.
00686824
Drops - Oral
1 DH / DH
12/31/1987
ROSMARINUS OFFICINALIS-INJEEL FORTE LIQ (6D,8D,12D,30D,200D/1.1ML)
02071878
Liquid - Oral
6 D / 1.1 ML
12/31/1994
UNDA 47
seroyal international inc.
02236593
Granules ,  Drops - Oral
6 X
4/6/1998
ROSMARINUS OFFICINALIS
dolisos canada inc.
02234710
Globules ,  Liquid ,  Granules - Oral
1 X
1/5/1998
HOMEOPATHIC MEDICINE (S61) DPS 30C
total health centre
02071282
Drops - Oral
30 C / ML
12/31/1994
DR SCHIEFFER NERVE HERB TEA NR 6
dr nachf dr. nachf grunitz chemische erzeugnisse
00113018
Leaf - Oral
10 %
12/31/1951
UNDA 11
seroyal international inc.
02233231
Tablet ,  Granules ,  Pellet ,  Drops ,  Liquid - Oral
4 X
4/6/1998
ROSMARINUS COMP.
02232735
Liquid - Oral
5 D
4/15/1998
#7 NERVE TEA
3 way herbs ltd.
01996878
Tea (Herbal) - Oral
4 %
12/31/1993

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
TUTUKON SOLUCION ORAL
Setonda S.L.
82648
SOLUCIÓN ORAL
Sin Receta
Commercialized

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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