Equate Everyday Clean Gentle Dandruff

Manufacturer
Wal-Mart Stores, Inc. | Apollo Health and Beauty Care Inc.
Effective date
2018-02-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:27

Label at a glance#

ProductEquate Everyday Clean Gentle Dandruff
Active ingredientPYRITHIONE ZINC
Label structure7 sections

Indications and uses

to help prevent recurrence of flaking and itching associated with dandruff.

Dosage and administration

For best results, use at least twice a week or as directed by a doctor. wet hair, massage onto scalp and rinse. repeat if desired.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

  • to help prevent recurrence of flaking and itching associated with dandruff.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use 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

  • In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For best results, use at least twice a week or as directed by a doctor.
  • wet hair, massage onto scalp and rinse.
  • repeat if desired.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Acrylates Copolymer, Cocamidopropyl Betaine, Sodium Chloride, Glycol Distearate, Laureth-4, Sodium Hydroxide, Polyquaternium-113, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone, Red 33 (CI 17200), Blue 1 (CI 42090)

Questions or comments?

OTC - QUESTIONS SECTION

1-888-287-1915

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of the labelimage of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN1
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD1
209884zinc pyrithione 1 % Medicated ConditionerSY1
209884zinc pyrithione 1 % Medicated ShampooSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-087-142024-01-30C16284748780-11030e365-3a39-111a-e063-dadaa90a10e2Drug Facts
49035-087-332024-01-30C16284748780-11030e365-3a39-111a-e063-dadaa90a10e2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-087-14Equate Everyday Clean Gentle Dandruff420 mL in 1 BOTTLE, PLASTICSHAMPOO4201
49035-087-33Equate Everyday Clean Gentle Dandruff1000 mL in 1 BOTTLE, PLASTICSHAMPOO10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-087EQUATE EVERYDAY CLEAN GENTLE DANDRUFF (PYRITHIONE ZINC) SHAMPOO [WAL-MART STORES, INC.]1Legacy NDC, 2 package rows20180210_d93bee03-8abd-42e8-838e-1d25b7c3ed31.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-08749035-087-33, 49035-087-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
0c6dd288-237c-45b3-bc73-59740ef29960d93bee03-8abd-42e8-838e-1d25b7c3ed312018-02-09WarningsExact identifier
spl id: 0c6dd288-237c-45b3-bc73-59740ef29960
spl set id: d93bee03-8abd-42e8-838e-1d25b7c3ed31

Reported adverse events (FAERS/openFDA)#

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