MedPath

Calendula officinalis whole

Generic Name
Calendula officinalis whole
Drug Type
Biotech
Unique Ingredient Identifier
PFR03EBU0H

Overview

Calendula officinalis whole 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.

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

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
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
CALENDULA OFFICINALIS GOUTTE 4CH-30CH
dolisos laboratoires s.a.
00680648
Drops - Oral
2 CH / CH
12/31/1987
IN GEL
bio active canada ltd.
02233627
Gel - Topical
1 X
5/26/1998
BR-NIX SPRAY
terra botanica products ltd.
02233303
Liquid - Topical
1 X
5/25/1998
APIZELEN
bio active canada ltd.
02233553
Liquid - Oral
2 C
5/26/1998
STOMACH TEA
3 way herbs ltd.
00582751
Tea (Herbal) - Oral
8 %
12/31/1983
TRAUMEEL
02232004
Tablet ,  Drops - Oral
2 D
8/28/1997
DR SCHIEFFER NERVE HERB TEA NR 6
dr nachf dr. nachf grunitz chemische erzeugnisse
00113018
Leaf - Oral
1 %
12/31/1951
CALENDULA B82
professional health products
02232186
Ointment - Topical
1 D
4/1/1998
CALENDULA OFFICINALIS
dolisos canada inc.
02234379
Granules ,  Globules ,  Liquid - Oral
1 X
1/5/1998
TRIFOLOPLEX
bio active canada ltd.
02233689
Liquid - Oral
1 X
5/26/1998

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.

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