MedPath

Capsicum oleoresin

Generic Name
Capsicum oleoresin
Brand Names
Previdolrx Analgesic Pak
Drug Type
Biotech
CAS Number
8023-77-6
Unique Ingredient Identifier
UW86K581WY

Overview

Capsicum oleoresin is an oily organic resin derived from the fruit of plants in the Capsicum genus, such as chilli peppers. When the plants are finely ground, capsicum oleoresin is formed after the extraction process of capsaicin using oragnic solvents such as ethanol. It is commonly used as a culinary spice. The intensity of biological actions and toxicological effects of capsicum oleoresin are a direct function of the amount of capsaicinoids, or capsaicin, present in the compound . Capsaicinoids comprise of a group of fat-soluble pungent chemical phenols and include Capsaicin, dihydrocapsaicin, nordihydrocapsaicin, homocapsaicin, and homodihydrocapsaicin . Capsaicin and dihydrocapsaicin are the most pungent capsaicinoid analogues . Capsicum oleoresin is contained in pepper sprays when suspended in water, and acts an active lachrymatory agent that induces irritation, lacrimation, pain, and temporary blindness when in contact with eyes. Due to its analgesic properties, capsicum oleoresin is used to temporarily relieve of minor aches and pains of muscles and joints as an active ingredient in topical OTC preparations and has been studied for management of different models of neuropathic pain . It is suggested that capsicum oleoresin is a rich source of phytochemicals that consist of phenolic compounds with antioxidant and antidiabetic activities .

Indication

Indicated for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains and sprains.

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2019/10/14
Phase 2
Active, not recruiting
Vastra Gotaland Region

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Puretek Corporation
59088-223
TOPICAL
0.5 mg in 1 g
2/28/2025

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
PainKlēn
484720
Medicine
A
3/31/2025
Athletes Gel
356163
Medicine
A
3/4/2021
TRANS WOOD LOCK LINIMENT
405750
Medicine
A
3/6/2023
Deep Heat Low Odour Relief
357357
Medicine
A
3/23/2021
Stiff Sore and Sorry Pain Relief and Injury
287338
Medicine
A
3/31/2017
Percutane Pain Relief Cream
199380
Medicine
A
7/17/2012
Magnesium+ Joint Lotion
464747
Medicine
A
10/17/2024

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
WATKINS ANALGESIC BALM
watkins incorporated
00376450
Cream - Topical
1 %
12/31/1977
HERBALAX FORTE NO 70 TAB
santé naturelle (ag) ltée
00511390
Tablet - Oral
1.62 MG
12/31/1981
BIOBALSAM
biopharmatech inc.
02230695
Cream - Topical
0.05 %
6/4/1997
HALF AND HALF BALM
mueller sports medicine, inc.
00240494
Ointment - Topical
794.5 G / 132 Kg
12/31/1970
BUCKLEY'S STAINLESS WHITE RUB
w.k. buckley ltd.
00360570
Ointment - Topical
2 MG / 28.3 G
12/31/1936
RHEUMALAN ONT
hilary's distibution ltd.
00398969
Ointment - Topical
295 MG / 28.3 G
12/31/1957

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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