Overview
Diethylamino hydroxybenzoyl hexyl benzoate is a UV filter with high absorption in the UV-A range. Minimizing the overexposure of human skin to ultraviolet radiation that may lead to acute and chronic photodamage, diethylamino hydroxybenzoyl hexyl benzoate is an oil-soluble UV filter that may be incorporated in the oil phase of emulsions . Diethylamino hydroxybenzoyl hexyl benzoate was approved in Europe in 2005, and is also marketed in the U.S., South America, Mexico, Japan and Taiwan. It has a chemical structure similar to the classical benxophoenone drug class, and displays good photostability . It is used in concentrations up to 10% in sunscreen products, either alone or in combination with other UV absorbers .
Indication
Indicated for use as a sunscreen agent.
Associated Conditions
- Sunburn
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 |
---|---|---|---|---|---|
THANK YOU FARMER CO., LTD. | 70618-010 | TOPICAL | 1.5 mg in 50 mL | 4/28/2025 |
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 |
---|---|---|---|---|---|
Cetaphil Sun Ultra-Light Lotion SPF50+ Body & Face | 286720 | Medicine | A | 3/14/2017 | |
QV FACE MOISTURISING DAY CREAM SPF 30 | 374097 | Medicine | A | 9/2/2021 | |
Sun Zapper Blue SPF50+ Zinc Stick | 279799 | Medicine | A | 8/31/2016 | |
Sun Zapper Extreme Zinc SPF 50+ Orange Sun | 391736 | Medicine | A | 7/4/2022 | |
Maxiblock Zinc Stick Tinted SPF50+ | 409827 | Medicine | A | 5/31/2023 | |
BONDI SANDS DAILY MOISTURISING FACE SPF 50+ FRAGRANCE FREE TINTED SUNSCREEN FLUID | 409066 | Medicine | A | 5/16/2023 | |
Surf Life Saving Tinted Zinc Stick SPF50+ | 410417 | Medicine | A | 6/13/2023 | |
Neutrogena Ultra Sheer Fluid Sunscreen Age Shield | 488906 | Medicine | A | 5/15/2025 | |
Sun Zapper SPF 50+ Yellow Zinc Stick | 487211 | Medicine | A | 4/30/2025 | |
Sun Zapper Yellow SPF50+ Zinc Stick | 282968 | Medicine | A | 11/28/2016 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
No Health Canada approvals found for this drug. |
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.