FDA.reportPublic FDA data

BlooSkim Anti Dandruff

Manufacturer
Good Manager Holdings Inc
Effective date
2024-11-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:49:58

Label at a glance#

ProductBlooSkim Anti Dandruff
Active ingredientKETOCONAZOLE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ketoconazole 1%

OTC - PURPOSE SECTION

ANTI-DANDRUFF SHAMPOO

INDICATIONS & USAGE SECTION

Controls flaking, scaling, and itching caused by dandruff

OTC - WHEN USING SECTION

When using this product

Avoid contact with eyes

If contact occurs, rinse thoroughly with water.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use

On scalp that is broken or inflamed

If you are allergic to ingredients in this product

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

OTC - STOP USE SECTION

Stop use and ask a doctor if

A rash appears.

Condition worsens or does not improve within 2-4 weeks.

If pregnant or breast-feeding, consult a doctor before use.

DOSAGE & ADMINISTRATION SECTION

Directions

adults and children 12 years and over

Wet hair thoroughly.

Apply shampoo, lather generously, and rinse thoroughly.

Repeat if necessary.

Use every 3-4 days for up to 8 weeks or as directed by a doctor.

Afterward, use as needed to control dandruff.

children under 12 years

Ask a doctor

OTHER SAFETY INFORMATION

Store at 20°C to 25°C (68°F to 77°F)

INACTIVE INGREDIENT SECTION

Citric Acid, Herba Violae, Euphorbia Hirta, Murraya Paniculata , Mentha Canadensis, Sophora Flavescens, Dittany Bark, Glabrous Greenbrier Rhizome, Mosla Cavaleriei Levl, Stellera Chamaejasme, Huang Bai, Sessile Stemona Root, Gleditsia Sinensis, Common Cnidium Fruit, Fructus Kochiae, Tea Tree Oil, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

anti dandruffanti dandruff

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82372-01382372-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
MURRAYA PANICULATA WHOLEY8ZAA3Z7WUIACT
MENTHA CANADENSIS WHOLEJ1BO4MHT2LIACT
GLEDITSIA SINENSIS WHOLEFS3UB95UTGIACT
WATER059QF0KO0RIACT
SMILAX GLABRA TUBERPES3YXA3LRIACT
MOSLA CAVALERIEI WHOLE05O8B64OS2IACT
VIOLA PHILIPPICA WHOLEO176VC3N54IACT
KETOCONAZOLER9400W927IACTIB
EUPHORBIA HIRTAL13YF113GNIACT
DICTAMNUS DASYCARPUS ROOT6153LEN214IACT
TEA TREE OILVIF565UC2GIACT
STELLERA CHAMAEJASME WHOLE80N0P0DD9JIACT
SOPHORA FLAVESCENS WHOLEX8KX602M5LIACT
CITRIC ACID2968PHW8QPIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
PHELLODENDRON CHINENSE WHOLEQKA3ZK8IIEIACT
STEMONA SESSILIFOLIA ROOTEKG8030U4NIACT
BASSIA SCOPARIA FRUIT04W97Z676YIACT

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
2deca703-b11b-de57-e063-6294a90ae5432625ef0c-61d0-ee5c-e063-6394a90a40372025-02-12WarningsExact identifier
spl set id: 2625ef0c-61d0-ee5c-e063-6394a90a4037

Reported adverse events (FAERS/openFDA)#

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