MedPath

Beeswax

Generic Name
Beeswax
Drug Type
Biotech
CAS Number
8012-89-3
Unique Ingredient Identifier
2ZA36H0S2V

Overview

The wax obtained from the honeycomb of the bee. It consists primarily of myricyl palmitate, cerotic acid esters and some high-carbon paraffins. Beeswax is used as a stiffening agent in ointments and creams, and enables water to be incorporated to produce water-in-oil emulsions. It is also used as a coating in the manufacture of modified-release oral preparations

Indication

Beeswax is also characterized by several therapeutic properties of great interest to us; it is thought to be particularly effective in healing bruises, inflammation and burns. Recently, the interest of researchers has moved even on antimicrobial properties of beeswax although there are still few studies in the literature focused only on the action of beeswax. The few studies showed an antimicrobic effectiveness of beeswax against overall Staphylococcus aureus, Salmonella enterica, Candida albicans and Aspergillus niger. A sterile preparation of white beeswax, hard paraffin, and isopropyl palmitate (Sterile Surgical Bone Wax) is used to control bleeding from damaged bone during surgery. It should not be confused with Aseptic Surgical Wax (BPC 1949), also known as Horsley's Wax , which contained yellow beeswax, olive oil, and phenol in a mercuric chloride solution and was used to control haemorrhage in bone or cranial surgery.

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
BIOCARE PLUS INTERNATIONAL LIMITED
85522-001
TOPICAL
0.17 g in 1 g
4/9/2025

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
Bexanol Beeswax Alcohol
319326
Medicine
A
6/27/2019
RAYDEL BEESWAX ALCOHOL CELL 100
463709
Medicine
A
10/3/2024
RAYDEL Beeswax alcohol cell 100
228101
Medicine
A
9/17/2014
ABEXOL
387559
Medicine
A
4/27/2022

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
HEM-RELIEF ONT
nature's way of canada ltd.
00656259
Ointment - Topical
0.6 %
12/31/1985
X-ITCH ONT
nature's way of canada ltd.
00656240
Ointment - Topical
.6 %
12/31/1986
FITE-BITE
nature's way of canada ltd.
00656232
Ointment - Topical
.6 %
12/31/1985

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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