Ecamsule

Overview

Ecamsule is an organic compound which is added to many sunscreens to filter out UVA rays. It is a benzylidene camphor derivative, many of which are known for their excellent photostability. Ecamsule has been approved for use in the U.S. since 2006, but only at a specific concentration and only in a few products manufactured by L'Oreal. The company got approval for those products through a new drug application process.

Indication

Applied topically to filter out UVA rays.

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
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
LA ROCHE-POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS DRY TOUCH GEL CREME TINTED SPF50+	297587	L'Oreal Australia Pty Ltd	Medicine	A	12/15/2017
LA ROCHE-POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS XL DRY TOUCH GEL-CREAM SPF50+	308621	L'Oreal Australia Pty Ltd	Medicine	A	8/24/2018
La Roche-Posay Laboratoire Dermatologique Anthelios XL Ultra-Light Spray SPF50+	300600	L'Oreal Australia Pty Ltd	Medicine	A	3/9/2018
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS KA+ SUNSCREEN SPF50+	404334	L'Oreal Australia Pty Ltd	Medicine	A	2/3/2023
ANTHELIOS UVMUNE 400 ULTRA INVISIBLE FLUID	495107	L'Oreal Australia Pty Ltd	Medicine	A	6/30/2025
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS ULTRA TINTED BB CREAM SPF50+	307005	L'Oreal Australia Pty Ltd	Medicine	A	7/13/2018
LA ROCHE-POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS DRY TOUCH GEL CREME SPF50+	297590	L'Oreal Australia Pty Ltd	Medicine	A	12/15/2017
LA ROCHE-POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS XL ULTRA LIGHT TINTED FLUID SPF50+	315642	L'Oreal Australia Pty Ltd	Medicine	A	3/22/2019
Cetaphil UVA / UVB Defence	294062	Galderma Australia Pty Ltd	Medicine	A	9/19/2017
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS ULTRA COMFORT NON PERFUMED CREAM SPF50+	307004	L'Oreal Australia Pty Ltd	Medicine	A	7/13/2018

Health Canada Drug Approvals

Approved Product	Company	DIN	Dosage Form	Strength	Market Date
SHEER LOTION SPF 45 BARE SKIN FEEL	vichy canada	02401924	Lotion - Topical	0.5 % / W/W	4/8/2013
ANTHELIOS ULTRA-FLUID LOTION	laboratoires la roche-posay canada	02364700	Lotion - Topical	2.00 % / W/W	4/13/2011
LAIT PROTECTEUR HYDRO-SATINANT SPF15	lancome canada	02207575	Lotion - Topical	.5 %	12/31/1996
FPS 60 CRÈME UV HYDRATANTE	vichy canada	02280388	Cream - Topical	2.00 % / W/W	4/20/2007
FPS 30 LAIT SOLAIRE	biotherm canada	02378485	Cream - Topical	0.5 % / W/W	3/26/2012
LANCOME LAIT ECRAN TOTAL HYDRO-SATIN.SPF25	lancome canada	02165856	Lotion - Topical	1 %	12/31/1995
LAIT SOLAIRE ECRAN TOTAL SPF 25	lancome canada	02233715	Liquid - Topical	1 %	3/16/1998
ULTRA-FLUID BODY MILK SUN PROTECTION SPF 30	biotherm canada	02296829	Lotion - Topical	0.25 %	4/1/2008
THERMAL S UV SPF 20	vichy canada	02243988	Cream - Topical	1.5 %	6/1/2001
OMBRELLE - LOTION ENFANTS SPF 30	ombrelle canada	02241278	Lotion - Topical	1.0 %	3/31/2000

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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