OREAD BLUE 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 23:37:57

Label at a glance#

ProductOREAD BLUE Anti-Dandruff
Active ingredientPYRITHIONE ZINC
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

Pyrithione Zinc .............. 2.00%

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, Aqua (Deionized Water), Cocamide MEA, Cocamidopropyl Betaine, Disodium Oleamido MEA Sulfosuccinate, Gluconolactone, Glycerin, Glyceryl Caprylate, Hydroxyethylcellulose, Magnesium Aluminum Silicate, Melaleuca Alternifolia (Tea Tree) Oil, PEG-12 Dimethicone, Polyquaternium-7, Propylene Glycol, Sodium Benzoate, Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Triethanolamine, FD&C Blue #1.

Questions?

OTC - QUESTIONS SECTION

1-833-673-2301 (M-F) (9-5pm CST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63015-24163015-241-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Source Document#

Source XML

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
07498503-b5b7-85bc-e063-6294a90a28c6222c3bc1-51f1-4040-be3d-8493fd07fcb62023-10-09WarningsExact identifier
spl set id: 222c3bc1-51f1-4040-be3d-8493fd07fcb6

Reported adverse events (FAERS/openFDA)#

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