FDA.reportPublic FDA data

OREAD GREEN Anti-Dandruff

Manufacturer
Oread Therapeutics, LLC
Effective date
2020-03-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:38:02

Label at a glance#

ProductOREAD GREEN Anti-Dandruff
Active ingredientSELENIUM SULFIDE
Label structure8 sections

Indications and uses

Reduces and controls skin and scalp itching, irritation, redness, flaking, and scaling associated with dandruff and seborrheic dermatitis.

Dosage and administration

For best results, use at least twice per week, or as directed by physician.  More detailed directions applicable to a particular product formulation may also be included.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Selenium Sulfide........... 1.00%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

Reduces and controls skin and scalp itching, irritation, redness, flaking, and scaling associated with dandruff and seborrheic dermatitis.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, rinse thoroughly with water

Stop and ask a doctor if

OTC - STOP USE SECTION

Condition worsens or does not improve after regular use of this product as directed.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For best results, use at least twice per week, or as directed by physician. 
  • More detailed directions applicable to a particular product formulation may also be included.

Other information

SPL UNCLASSIFIED SECTION

  • Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates Copolymer, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Aqua (Deionized Water), Cocamide MEA, Cocamidopropyl Betaine, Dimethicone, Gluconolactone, Glycerin, Glyceryl Caprylate, Lavandula Angustifolia (Lavender) Oil, Magnesium Aluminum Silicate, Melaleuca Alternifolia (Tea Tree) Oil, PEG-12 Sodium Hydroxide, Sodium Benzoate, FD&C Blue #1.

Questions?

OTC - QUESTIONS SECTION

1-833-673-2301 (M-F) (9-5pm CST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63015-24363015-243-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
AMMONIUM LAURYL SULFATEQ7AO2R1M0BIACT
WATER059QF0KO0RIACT
COCO MONOETHANOLAMIDEC80684146DIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
DIMETHICONE92RU3N3Y1OIACT
GLUCONOLACTONEWQ29KQ9POTIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
LAVENDER OILZBP1YXW0H8IACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
TEA TREE OILVIF565UC2GIACT
SODIUM BENZOATEOJ245FE5EUIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
SELENIUM SULFIDEZ69D9E381QACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
07497a80-1126-b00e-e063-6394a90a054e8ea3a8b4-3b71-425b-992e-bdd7c46e0ac42023-10-09WarningsExact identifier
spl set id: 8ea3a8b4-3b71-425b-992e-bdd7c46e0ac4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.