FDA.reportPublic FDA data

Lacura Everyday Clean Dandruff

Manufacturer
Aldi
Effective date
2021-05-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:44:43

Label at a glance#

ProductLacura Everyday Clean Dandruff
Active ingredientPYRITHIONE ZINC
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 1%

OTC - PURPOSE SECTION

Anti-dandruff

INDICATIONS & USAGE SECTION

Helps prevent recurrence of flaking and itching associated with dandruff.

WARNINGS SECTION

For external use only. When using the product do not get into eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and ask a doctor if conditions worsens or does not improve after regular use as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Shake well. For maximum dandruff control, use every time you shampoo. Wet hair, massage onto scalp, rinse, repeat if desired. For best results use at least twice a week or as directed by a doctor.

INACTIVE INGREDIENT SECTION

Water, sodium laureth sulfate, cocamidopropyl betaine, sodium lauryl sulfate, cocamide MEA, glycol distearate, laureth-4, dimethiconol, zinc PCA, sodium chloride, sodium xylenesulfonate, fragrance, sodium benzoate, TEA-dodecylbenzenesulfonate, guar hydroxypropyltrimonium chloride, polyquaternium-10, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64024-00564024-005-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
PYRITHIONE ZINCR953O2RHZ5ACTIB
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM XYLENESULFONATEG4LZF950URIACT
POLYQUATERNIUM-10 (400 MPA.S AT 2%)HB1401PQFSIACT
GLYCOL DISTEARATE13W7MDN21WIACT
DIMETHICONOL (2000 CST)T74O12AN6YIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM LAURYL SULFATE368GB5141JIACT
LAURETH-46HQ855798JIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
TRIETHANOLAMINE DODECYLBENZENESULFONATE8HM7ZD48HNIACT
SODIUM CHLORIDE451W47IQ8XIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
COCO MONOETHANOLAMIDEC80684146DIACT
ZINC PIDOLATEC32PQ86DH4IACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT

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
eb7b0739-3eec-4598-e053-2a95a90a8d53c1fbfcf9-85b8-1b74-e053-2a95a90ac1912022-10-20WarningsExact identifier
spl set id: c1fbfcf9-85b8-1b74-e053-2a95a90ac191

Reported adverse events (FAERS/openFDA)#

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