Redken Brews NYC Grooming Pyrithione Zinc Anti-dandruff

Manufacturer
L'Oreal USA Products Inc | L'OREAL USA, INC. | Unette Corporation
Effective date
2020-11-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:08:32

Label at a glance#

ProductRedken Brews NYC Grooming Pyrithione Zinc Anti-dandruff
Active ingredientPYRITHIONE ZINC
Label structure11 sections

Indications and uses

for the relief of the symptoms of dandruff helps prevent recurrence of the symptoms of dandruff controls scalp itching, irritation, redness, flaking, and scaling associated with dandruff

Dosage and administration

for best results, use at least twice a week or as directed by a doctor shake well before each use wet hair and apply a small amount of shampoo apply evely to scalp, leave on for several minutes, and then rinse off

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

  • for the relief of the symptoms of dandruff
  • helps prevent recurrence of the symptoms of dandruff
  • controls scalp itching, irritation, redness, flaking, and scaling associated with dandruff

Warnings

WARNINGS SECTION

For external use only

Ask a doctor before use

OTC - ASK DOCTOR SECTION

in children under 2 years of age

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a physician if

OTC - STOP USE SECTION

condition worsens or does not improve after regular use

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 a week or as directed by a doctor
  • shake well before each use
  • wet hair and apply a small amount of shampoo
  • apply evely to scalp, leave on for several minutes, and then rinse off

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sodium laureth sulfate, sodium lauryl sulfate, glycerin, cocamide MEA, glycol distearate, sodium chloride, hexylene glycol, dimethicone, citric acid, fragrance, sodium benzoate, sodium hydroxide, coco-betaine, carbomer, guar hydroxypropyltrimonium chloride, menthoxypropanediolm sodium polynaphthalenesulfonate, salicylic acid, hydrolyzed soy protein, eugenol, limonene, cellulose gum, lecithin, fumaric acid, phosphoric acid, lavandula angustifolia (lavender) oil, methylisothiazolinone

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-18349967-183-01, 49967-183-02, 49967-183-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
6acd3372-185e-4bb6-8d44-5718695ed9e01fa0008d-16ad-441d-a7e4-543d7e66da0e2021-05-20WarningsExact identifier
spl set id: 1fa0008d-16ad-441d-a7e4-543d7e66da0e

Reported adverse events (FAERS/openFDA)#

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