LOCOID

This brand name is authorized in United States. It is also authorized in Finland, France, Ireland, Japan, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, South Africa, UK.

Active ingredients

The drug LOCOID contains one active pharmaceutical ingredient (API):

1	Hydrocortisone butyrate UNII 05RMF7YPWN - HYDROCORTISONE BUTYRATE
	Hydrocortisone butyrate is the butyrate salt form of hydrocortisone, a synthetic glucocorticoid receptor agonist with antiinflammatory, antipruritic and vasoconstrictive effects. Binding and activation of the glucocorticoid receptor results in the activation of lipocortin that in turn inhibits cytosolic phospholipase A2.
	Read more about Hydrocortisone butyrate

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
LOCOID Cream	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)
LOCOID Lotion, 0.1%	MPI, US: SPL/PLR	FDA, National Drug Code (US)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
D07AB02	Hydrocortisone butyrate	D Dermatologicals → D07 Corticosteroids, dermatological preparations → D07A Corticosteroids, plain → D07AB Corticosteroids, moderately potent (group II)
Discover more medicines within D07AB02

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
FI	Lääkealan turvallisuus- ja kehittämiskeskus	080456, 114761, 140013, 196889, 380922, 400422, 426573, 438591, 443227, 504502, 563799
FR	Base de données publique des médicaments	60676481, 63947112, 66423894, 66841235, 67369944
GB	Medicines & Healthcare Products Regulatory Agency	180625, 21707, 33564, 33574, 37791, 40194
IE	Health Products Regulatory Authority	19933, 63932, 65927, 65935
JP	医薬品医療機器総合機構	2646717M1096, 2646717N1083
MT	Medicines Authority	MA1456/00301, MA1456/00302, PI908/03603A, PI908/03604A
MX	Comisión Federal para la Protección contra Riesgos Sanitarios	77056
NL	Z-Index G-Standaard	12130648, 12130699, 12357707, 12895385, 13814214
NL	Z-Index G-Standaard, PRK	39187, 6076, 63053, 63061
NZ	Medicines and Medical Devices Safety Authority	2123, 2124, 2126, 2128
PL	Rejestru Produktów Leczniczych	100039476, 100039482, 100039499, 100246620, 100361404, 100399424, 100451183
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W67758001, W67759001
US	FDA, National Drug Code	16781-382, 16781-384, 16781-391, 16781-392
ZA	Health Products Regulatory Authority	34/13.4.1/0221, H/13.4.1/107, H/13.4.1/108, H/13.4.1/109, W/13.4.1/355