FDA.reportPublic FDA data

Walmart

Manufacturer
Wal-Mart Stores, Inc | Apollo Health and Beauty Care Inc. | Apollo Health and Beauty Care Inc
Effective date
2024-10-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:51:48

Label at a glance#

ProductWalmart
Active ingredientPYRITHIONE ZINC
Label structure8 sections

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc

OTC - PURPOSE SECTION

For the relief of itching, redness and flaking associated with dandruff

WARNINGS SECTION

For External use

OTC - DO NOT USE SECTION

on children under 2 years of age, unless directed by a doctor.

OTC - STOP USE SECTION

Stop use and ask a doctor ifcondition worsens or does not improve after regular use of this product
as directed.

OTC - WHEN USING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a poison control centre or get medical help right away.

DOSAGE & ADMINISTRATION SECTION

• Adults and children 2 years and older.

  • Wet Scalp. Apply evenly to scalp, leave on for several minutes, and then rinse off. Use at least twice per week or as

directed by a doctor or pharmacist.

INDICATIONS & USAGE SECTION

Relieves itching , redness and flakes associated with Dandruff.

INACTIVE INGREDIENT SECTION

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

STORAGE AND HANDLING SECTION

Store at room temperature

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

950 mL950 mL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79903-897WALMART (PYRITHIONE ZINC) LOTION/SHAMPOO [WAL-MART STORES, INC]2Legacy NDC20241022_ecab59d4-1f09-ef9e-e053-2995a90a0781.zip

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
79903-89779903-897-95

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
WATER059QF0KO0RIACT
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)74G4R6TH13IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
DIMETHICONE92RU3N3Y1OIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
LAURETH-46HQ855798JIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
ACID RED 337 FREE ACIDZ9C910400YIACT
DIRECT BLUE 18NN34MAQ6HIACT
POLYQUATERNIUM-11 (1000000 MW)0B44BS5IJSIACT
GLYCOL DISTEARATE13W7MDN21WIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM HYDROXIDE55X04QC32IIACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE15O9QS218WIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB

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
5117acf0-3ac5-705b-e063-6394a90a6debecab59d4-1f09-ef9e-e053-2995a90a07812026-05-05WarningsExact identifier
spl set id: ecab59d4-1f09-ef9e-e053-2995a90a0781

Reported adverse events (FAERS/openFDA)#

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