THE ORDINARY SULFUR 10% POWDER-TO-CREAM CONCENTRATE- sulfur powder

The Ordinary Sulfur 10% Powder-to-Cream Concentrate by

Drug Labeling and Warnings

The Ordinary Sulfur 10% Powder-to-Cream Concentrate by is a Otc medication manufactured, distributed, or labeled by Deciem. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

PURPOSE

INACTIVE INGREDIENT

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

THE ORDINARY SULFUR 10% POWDER-TO-CREAM CONCENTRATE 
sulfur powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72208-588
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	1.5 mg  in 15 mg

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
CHLORPHENESIN (UNII: I670DAL4SZ)
NIACINAMIDE (UNII: 25X51I8RD4)
GLYCERIN (UNII: PDC6A3C0OX)
PROPANEDIOL (UNII: 5965N8W85T)
AQUA (UNII: 059QF0KO0R)
ACACIA SENEGAL GUM (UNII: 5C5403N26O)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CARNITINE (UNII: S7UI8SM58A)
POLY-L-LYSINE (30000-70000 MW) (UNII: 0A1V8JTU2M)
KAOLIN (UNII: 24H4NWX5CO)
CITRIC ACID (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72208-588-01	1 in 1 BOX	07/28/2025
1		5000 mg in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	07/28/2025

Labeler - Deciem (203133665)