FDA.reportPublic FDA data

Purple Dandruff Conditioner

Manufacturer
Guangzhou Nawei Beauty Biotechnology Co., Ltd
Effective date
2025-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:33:30

Label at a glance#

ProductPurple Dandruff Conditioner
Active ingredientCETEARYL ALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


CETEARYL ALCOHOL

OTC - PURPOSE SECTION

exclusive purple conditioner effectively inhibits the growth of scalp fungi

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

INDICATIONS & USAGE SECTION

After washing your hair,apply the conditioner evenly to your hair until your hair is wrapped in the conditioner,

WARNINGS SECTION

CAUTION:For external use only

DOSAGE & ADMINISTRATION SECTION

Size:16.91 fl oz/500ml

INACTIVE INGREDIENT SECTION


CETYL ALCOHOL,AMINOETHYLAMINOPROPYL DIMETHICONE,
CETEARTRIMONIUM CHLORIDE,GLYCERIN,CYCLOPENTASILOXANE,
DIMETHICONOL,FRAGRANCE,BEHENTRIMONIUM CHLORIDE,
HYDROXYETHYLCELLULOSE,CITRIC ACID,UTYROSPERMUM PARKII(SHEA)FRUIT EXTRACT,
ROSMARINUS OFFICINALIS ROSEMARY) EXTRACT,PANAX GINSENG ROOT EXTRACT,
CAFFEINE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

22

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85605-456-12Purple Dandruff Conditioner1 in 1 BOTTLELIQUID11
85605-456-12Purple Dandruff Conditioner2 in 1 BOXLIQUID21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85605-456PURPLE DANDRUFF CONDITIONER LIQUID [GUANGZHOU NAWEI BEAUTY BIOTECHNOLOGY CO., LTD]12 package rows20250502_34019bd1-8a20-1522-e063-6394a90a5f3c.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
85605-45685605-456-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETYL HYDROXYETHYLCELLULOSE (550000 MW)2MIM45ZIL3IACT
CETEARYL ALCOHOL2DMT128M1SACTIB
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
CITRIC ACID2968PHW8QPIACT
CETYL ALCOHOL936JST6JCNIACT
GLYCERINPDC6A3C0OXIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
CETEARTRIMONIUM CHLORIDE34L9KA56IOIACT
FRAGRANCE GREEN APPLE ORC2001072U9GH30P956IACT
DIMETHICONOL (40 CST)343C7U75XWIACT
CAFFEINE3G6A5W338EIACT

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
34019bd1-8a21-1522-e063-6394a90a5f3c34019bd1-8a20-1522-e063-6394a90a5f3c2025-04-30WarningsExact identifier
spl id: 34019bd1-8a21-1522-e063-6394a90a5f3c
spl set id: 34019bd1-8a20-1522-e063-6394a90a5f3c

Reported adverse events (FAERS/openFDA)#

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