FDA.reportPublic FDA data

Purple Dandruff

Manufacturer
Guangzhou Nawei Beauty Biotechnology Co., Ltd
Effective date
2025-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:33:29

Label at a glance#

ProductPurple Dandruff
Active ingredientCOCAMIDE MEA
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


SODIUM LAURETH SULFATE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

INDICATIONS & USAGE SECTION

After moisturizing the hair and scalp thoroughly with warm water,rub an appropriate amount of this product in the palm of your hand until it foams,then apply it to the hair,gently leave it for 2 to 5 minutes.

WARNINGS SECTION

CAUTION:For external use only.

DOSAGE & ADMINISTRATION SECTION

Size:16.91 fl oz/500ml

INACTIVE INGREDIENT SECTION


COCAMIDOPROPYL BETAINE,DIMETHICONE,DIOLEOYLETHYL HYDROXYETHYLMONIUM METHOSULFATE,
AMMONIUM LAURYL SULFATE,COCAMIDE MEA,
GLYCERIN,DIMETHICONOL,SODIUM LAURYL SULFATE,COCAMIDE METHYL MEA,FRAGRANCE,SODIUM CHLORIDE,
GLYCINE,GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE,PALMITAMIDOPROPYLTRIMONIUM CHLORIDE,ALLANTOIN
SALICYLIC ACID,CITRIC ACID,BIOTIN,CASTOR OIL,MELALEUCA ALTERNIFOLIA(TEATREE)LEAF OIL,
MENTHA HAPLOCALYX OIL,HYDROLYZED RICE EXTRACT,ARGANIA SPINOSA KERNEL OIL,

ELAEIS GUINEENSIS(PALM)KERNEL OIL

OTC - PURPOSE SECTION

purple anti-dandruff shampoo provides nutrition to hair and solves problems such as severe dandruff,seborrheic dermatitis,folliculitis and psoriasis

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85605-123-12Purple Dandruff1 in 1 BOTTLESHAMPOO11
85605-123-12Purple Dandruff2 in 1 BOXSHAMPOO21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85605-123PURPLE DANDRUFF (PURPLE DANDRUFF SHAMPOO) SHAMPOO [GUANGZHOU NAWEI BEAUTY BIOTECHNOLOGY CO., LTD]12 package rows20250501_33f5375e-6aab-792f-e063-6294a90a3f14.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85605-12385605-123-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCAMIDE MEAC80684146DACTIB
DIMETHICONOL (70 CST)MOT8IL21ARIACT
ELAEIS GUINEENSIS (PALM) KERNEL OILB0S90M0233IACT
AMMONIUM LAURYL SULFATEQ7AO2R1M0BIACT
ARGANIA SPINOSA KERNEL OIL4V59G5UW9XIACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDEB16G315W7AIACT
CITRIC ACID2968PHW8QPIACT
BIOTIN6SO6U10H04IACT
GLYCERINPDC6A3C0OXIACT
CASTOR OILD5340Y2I9GIACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OILVIF565UC2GIACT
DIOLEOYLETHYL HYDROXYETHYLMONIUM METHOSULFATE5UXX651CBSIACT
SODIUM LAURYL SULFATE368GB5141JIACT
ALLANTOIN344S277G0ZIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
COCAMIDE METHYL MEA79G1T427CFIACT
SODIUM CHLORIDE451W47IQ8XIACT
FRAGRANCE 135765EM498GW35IACT
DIMETHICONE 1000MCU2324216IACT
PALMITAMIDOPROPYLTRIMONIUM CHLORIDEN2U96D202FIACT

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
33f5375e-6aac-792f-e063-6294a90a3f1433f5375e-6aab-792f-e063-6294a90a3f142025-04-29WarningsExact identifier
spl id: 33f5375e-6aac-792f-e063-6294a90a3f14
spl set id: 33f5375e-6aab-792f-e063-6294a90a3f14

Reported adverse events (FAERS/openFDA)#

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