Overview
Benzoin is a white crystalline compound prepared by condensation of benzaldehyde in potassium cyanide, and is used in organic syntheses. This should not be confused with benzoin gum from STYRAX (see Benzoin resin). Benzoin is an FDA-approved colour additive used for marking fruits and vegetables.
Indication
No approved therapeutic indications.
Associated Conditions
- Bandage adhesion
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 |
|---|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|
| FreeMovement | 161667 | Medicine | A | 5/8/2009 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| BENZOINSPRAY - AER 25% | 02177447 | Aerosol - Topical | 25 % | 9/29/1997 | |
| COMPOUND BENZOIN TINCTURE USP | medi-flex inc. | 02117932 | Tincture - Topical | 10 % | 8/31/1998 |
| ONE TIME COMPOUND BENZOIN TCT F466 | ACME UNITED CORPORATION | 00518301 | Stick - Topical | 10 % | 12/31/1979 |
| HOMEOPATHIC MEDICINE (S #411) - 30C LIQ | total health centre | 02104660 | Liquid - Sublingual | 30 C / ML | 12/31/1994 |
| COLD SORE LOTION | stanley pharmaceuticals, a division of vita health products inc. | 00558559 | Lotion - Topical | 94 % | 12/31/1982 |
| COLD SORE LOTION | d.c. labs limited | 00096075 | Lotion - Topical | 2.505 G / 100 ML | 12/31/1966 |
| TUFFNER LIQUID | mueller sports medicine, inc. | 00240583 | Tincture - Topical | 11.25 GAL / 216 L | 12/31/1970 |
| CHASE COLDSOREX | Stella Pharmaceutical Canada Inc. | 02231933 | Liquid - Topical | 12.46 % | 12/30/1973 |
| TUFFNER CLEAR SPRAY | mueller sports medicine, inc. | 00240575 | Aerosol - Topical | 3 % | 12/31/1970 |
| COMPOUND BENZOIN TINCTURE | ACME UNITED CORPORATION | 00403644 | Liquid - Topical | 10 % | 12/31/1977 |
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.