FDA.reportPublic FDA data

Walmart

Manufacturer
Wal-Mart Stores, Inc | Apollo Health and Beauty Care Inc.
Effective date
2025-01-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:43:33

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 - WHEN USING SECTION

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years and older.
  • Shake well.
  • 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.

INACTIVE INGREDIENT SECTION

Water, Stearyl Alcohol, Behentrimonium Chloride, Cetyl Alcohol, Cocos Nucifera (Coconut) Oil,
Dimethicone, Fragrance, PPG-3 Benzyl Ether Ethylhexanoate, Lauryl PEG/PPG-18/18 Methicone,
Hydroxyethylcellulose, Sodium Hydroxide, Citric Acid, Methylchloroisothiazolinone,
Methylisothiazolinone.

STORAGE AND HANDLING SECTION

Store at room temperature

INDICATIONS & USAGE SECTION

Relieves itching , redness and flakes associated with Dandruff.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

700 mL700 mL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79903-899WALMART (PYRITHIONE ZINC) LOTION/SHAMPOO [WAL-MART STORES, INC]2Legacy NDC20250106_ecaab315-3bfa-beeb-e053-2a95a90aa411.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79903-89979903-899-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE15O9QS218WIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
LAURYL PEG/PPG-18/18 METHICONEZJ5S27D9NXIACT
CETYL HYDROXYETHYLCELLULOSE (350000 MW)T7SWE4S2TTIACT
STEARYL ALCOHOL2KR89I4H1YIACT
SODIUM HYDROXIDE55X04QC32IIACT
PPG-3 BENZYL ETHER ETHYLHEXANOATE3N703GY99WIACT
WATER059QF0KO0RIACT
CETYL ALCOHOL936JST6JCNIACT
COCONUT OILQ9L0O73W7LIACT
DIMETHICONE92RU3N3Y1OIACT
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
5117ce41-38c0-569a-e063-6394a90a6123ecaab315-3bfa-beeb-e053-2a95a90aa4112026-05-05WarningsExact identifier
spl set id: ecaab315-3bfa-beeb-e053-2a95a90aa411

Reported adverse events (FAERS/openFDA)#

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