FDA.reportPublic FDA data

Equate Dry Scalp Dandruff

Manufacturer
Wal-Mart Stores Inc | Apollo Health and Beauty Care Inc.
Effective date
2018-02-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:23

Label at a glance#

ProductEquate Dry Scalp Dandruff
Active ingredientPYRITHIONE ZINC
Label structure7 sections

Indications and uses

to help prevent reccurence 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 reccurence 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 ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Acrylates Copolymer, Cocamidopropyl Betaine, Prunus Amygdalus (Sweet Almond) Oil, Sodium Chloride, Glycol Distearate, Laureth-4, Sodium Hydroxide, Polyquaternium-113, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone.

Questions?

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
49035-086-232024-01-30C16284748780-11030e365-22ae-111a-e063-dadaa90a10e2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-086-23Equate Dry Scalp Dandruff701 mL in 1 BOTTLE, PLASTICSHAMPOO7011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-086EQUATE DRY SCALP DANDRUFF (PYRITHIONE ZINC) SHAMPOO [WAL-MART STORES INC]1Legacy NDC, 1 package rows20180206_d33f26a5-e16d-44b0-aa13-58e710e1bcfa.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-08649035-086-23

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
PYRITHIONE ZINCR953O2RHZ5ACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)74G4R6TH13IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
ALMOND OIL66YXD4DKO9IACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCOL DISTEARATE13W7MDN21WIACT
LAURETH-46HQ855798JIACT
SODIUM HYDROXIDE55X04QC32IIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT

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
ace9b879-f2fb-4c0f-b046-e69d7340dd9bd33f26a5-e16d-44b0-aa13-58e710e1bcfa2018-02-05WarningsExact identifier
spl id: ace9b879-f2fb-4c0f-b046-e69d7340dd9b
spl set id: d33f26a5-e16d-44b0-aa13-58e710e1bcfa

Reported adverse events (FAERS/openFDA)#

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