Anti-Dandruff

Manufacturer
Shenzhen Derbit Technology Co., Ltd.
Effective date
2024-01-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:07:32

Label at a glance#

ProductAnti-Dandruff
Active ingredientPYRITHIONE ZINC, AMMONIUM LAURYL SULFATE
Label structure12 sections

Storage and handling

n/a

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

ZINC PYRITHION (0.384%)

AMMONIUM LAURYL SULFATE (3.22%)

purpose

OTC - PURPOSE SECTION

Anti-dandruff

Detergent

use

INDICATIONS & USAGE SECTION

Wet your hair first, then pour the shampoo into your hands, rub it and use it on your hair

Warning

WARNINGS SECTION

If shampoo accidentally gets into your eyes, rinse your eyes immediately with water,If your scalp feels uncomfortable after use, please stop using it immediately

Do not use

OTC - DO NOT USE SECTION

Please do not use if you are allergic or itchy after use.

When using SECTION

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC-STOP USE SECTION

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 right away.

Direction

DOSAGE & ADMINISTRATION SECTION

n/a

STORAGE AND HANDLING SECTION

n/a

inactive ingredients

INACTIVE INGREDIENT SECTION

CAMELLIA JAPONICA SEED OIL

CAMELLIA SINENSIS LEAF EXTRACT

GLYCERIN

GLEDITSIA SINENSIS EXTRACT

HYDROGENATED CASTOR OIL

WATER

ZINGIBER OFFICINALE EXTRACT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83619-002-0183619-002-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83619-002-012025-07-29C16284748780-13b156c62-3079-fb37-e063-e6dba90a4e070e1a3a4a-3370-b484-e063-6294a90afe77

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83619-002-01Anti-Dandruff250 mL in 1 BOXSHAMPOO2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83619-002ANTI-DANDRUFF (ANTI-DANDRUFF SHAMPOO) SHAMPOO [SHENZHEN DERBIT TECHNOLOGY CO., LTD.]21 package rows20240119_0e1a3a4a-3370-b484-e063-6294a90afe77.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83619-00283619-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
0ea26fe5-c013-f13b-e063-6294a90adf8a0e1a3a4a-3370-b484-e063-6294a90afe772024-01-10WarningsExact identifier
spl id: 0ea26fe5-c013-f13b-e063-6294a90adf8a
spl set id: 0e1a3a4a-3370-b484-e063-6294a90afe77

Reported adverse events (FAERS/openFDA)#

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