SULPHOREC

This brand name is authorized in Nigeria.

Active ingredients

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

1	Sulfur UNII 70FD1KFU70 - SULFUR
	Read more about Sulfur

Packages

This drug has been approved in Nigeria as follows:

Identifier	Form	Presentation	Description	Approval
04-5175	Ointment	Sulphorec Ointment OINTMENT 10%;10%; 80% 1 x 30 g (in Alu tube)	Semi Solid Cream Yellow colored smooth ointment SULPHOREC OINTMENT PRECIPITATED SULFUR USP 10% W/W, MINERAL OIL USP 10% W/W, WHITE OINTMENT USP 80% W/W Precipitated Sulfur USP - 10% w/w, Mineral Oil USP -10% w/w, White Ointment USP - 80% w/w Apr-75 Drugs Imported Products 30G Over The Counter (OTC) 19/08/2021 GOLDMOORE INTERNATIONAL LIMITED, IDUMOBA LANE, IDUMOTA LAGOS LAGOS 18959076 goldmooreregulatory@gmail.com M/S YASH MEDICARE PVT. LTD, Nr. SABAR DAIRY, TALOD ROAD, PO. HAJIPUR, T.A. HIMATNAGAR – 383 006, GUJARAT, INDIA, India	26/04/2023

Medicine classification

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

ATC Group		Classification
D10AB	Preparations containing sulfur	D Dermatologicals → D10 Anti-acne preparations → D10A Anti-acne preparations for topical use
Discover more medicines within D10AB

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
NG	Registered Drug Product Database	04-5175