FDA.reportPublic FDA data

Anti Dandruff - Guangzhou ChuanMa International Trading Co.,Ltd.

Manufacturer
Guangzhou ChuanMa International Trading Co.,Ltd.
Effective date
2026-08-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-25 01:02:58

Label at a glance#

ProductAnti Dandruff
Active ingredientKETOCONAZOLE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ketoconazole 1%.
PurposeAnti-dandruff

OTC - PURPOSE SECTION

Use
controls flaking, scaling and itching asso-
ciated withdandruff

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical helpor contact a Poison Control Center right away.

WARNINGS SECTION

Warnings
For external use only
Do not use
on scalp that is broken or inflamed
on children under 12 years of age unless directed by a doctor

DOSAGE & ADMINISTRATION SECTION

Repeat. use every 3-4 days for up to 8 week

INDICATIONS & USAGE SECTION

Directions
adults and children 12 years and older: wet hair
thoroughly, apply shampoo, generously lather, rinse
thoroughly. Repeat.
use every 3-4 days for up to 8 weeks or as directed
by a doctor. Then use only as needed to control
dandruff.

INACTIVE INGREDIENT SECTION

Inactive ingredients
Aqua, Sodium Laureth Sulfate, Cocamide DEA, SodiumChloride, Cocamidopropyl Betaine, Ammonium LaurylSulfate, Polyquaternium-10, Fragrance, Phenoxyethanol,PEG-7 Glyceryl Cocoate, Bis-Aminopropyl Dimethicone,Hydroxypropyl Guar Hydroxypropyltrimonium Chloride,C12-13 Pareth-3, Lactate, Citric Acid, C11-15 Pareth-9,Trideceth-12, Sodium Benzoate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

85593-122-01标签85593-122-01标签

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85593-12285593-122-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
KETOCONAZOLER9400W927IACTIB
AQUA059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCAMIDE DEA92005F972DIACT
SODIUM CHLORIDE451W47IQ8XIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
AMMONIUM LAURYL SULFATEQ7AO2R1M0BIACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
FRAGRANCE FLORAL ORC0902236R66Z4YW3X0IACT
PHENOXYETHANOLHIE492ZZ3TIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
AMINOPROPYL DIMETHICONE (1000 MPA.S)P4P48I53XHIACT
HYDROXYPROPYL GUAR HYDROXYPROPYLTRIMONIUM CHLORIDEMVW5LK6LFTIACT
C12-13 PARETH-3DMC6N3419LIACT
LACTIC ACID33X04XA5ATIACT
CITRIC ACID2968PHW8QPIACT
C11-15 PARETH-9U6S376X80DIACT
TRIDECETH-12YFY3KG5Y7OIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
Anti DandruffKETOCONAZOLEGuangzhou ChuanMa International Trading Co.,Ltd.59a0a062-92d1-210a-e063-6394a90a9bf92026-08-22WarningsExact identifier
ndc (package): 85593-122-01
ndc (product): 85593-122
ndc11 (package): 85593012201
spl id: 59a0a062-92d2-210a-e063-6394a90a9bf9
spl set id: 59a0a062-92d1-210a-e063-6394a90a9bf9

Reported adverse events (FAERS/openFDA)#

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