FDA.reportPublic FDA data

anti-dandruff

Manufacturer
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Effective date
2025-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:06:54

Label at a glance#

Productanti-dandruff
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

1. For best results, use at least twice a week or as directed by a doctor 2. Wet hair thoroughly, massage shampoo into scalp, leave on for 3-5 minutes to allow maximum absorption. Then rinse thoroughly and repeat as needed

Storage and handling

No Data

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 3%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use

INDICATIONS & USAGE SECTION

Helps prevent recurrence of the scalp: irritation,
itching, redness, flaking and scaling associated with
dandruff

Warnings

WARNINGS SECTION

For external use only
Consult a doctor before use if you
■ are allergic to ingredients in this product
When using this product
■ avoid contact with eyes
■ if contact occurs, rinse eyes thoroughly with water
Stop use and consult a doctor if
■ condition worsens or does not improve after regular use of this product as directed

Do not use

OTC - DO NOT USE SECTION

Do not use if allergic to the ingredients in this product

OTC - WHEN USING SECTION

1. avoid contact with eyes
2. if contact occurs, rinse eyes thoroughly with water



OTC - STOP USE SECTION

condition worsens or does not improve after regular use of this product as directed

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

Directions

DOSAGE & ADMINISTRATION SECTION

1. For best results, use at least twice a week or as directed by a doctor
2. Wet hair thoroughly, massage shampoo into scalp, leave on for 3-5 minutes to allow maximum
absorption. Then rinse thoroughly and repeat as needed

Other information

STORAGE AND HANDLING SECTION

No Data

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Sodium Lauroyl Sarcosinate, Cocamidopropyl Betaine, Lauramidopropyl Betaine,Lecithin, Coco-Glucoside, Peg-120
MethyI Glucose Dioleate, Aloe Barbadensis Leaf Extract, HydroxyphenyI Propamidobenzoic Acid, Phenoxyethanol,
Menthol, Polyquaternium 10, Panthenol, Maltooligosyl Glucoside, Lindera Strychnifolia Extract, Carbomer, Piroctone
Olamine, Glycerin, Biotin, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Thuja Orientalis Leaf Extract, Panax Ginseng Root Extract,
Angelica Sinensis Extract, Zingiber Officinale (Ginger) Root Extract, Polygonum Multiflorum Extract, Rosmarinus
Officinalis (Rosemary) Leaf Extract, Fragrance, O-Cymen-5-Ol, Hydroxypropyltrimonium Hyaluronate, C12-15 Pareth-3,
Hydroxypropyltrimonium Hydrolyzed Collagen

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
205023salicylic acid 3 % Medicated ShampooPSN1
205023salicylic acid 30 MG/ML Medicated ShampooSCD1
205023salicylic acid 3 % Medicated ShampooSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84558-010-01anti-dandruff300 mL in 1 BOTTLESHAMPOO3001

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84558-01084558-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
LECITHIN, SUNFLOWER834K0WOS5GIACT
COCO-GLUCOSIDEICS790225BIACT
AQUA059QF0KO0RIACT
CARBOMER0A5MM307FCIACT
PIROCTONE OLAMINEA4V5C6R9FBIACT
C12-15 PARETH-3459EF9MP3YIACT
SODIUM LAUROYL SARCOSINATE632GS99618IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURAMIDOPROPYL BETAINE23D6XVI233IACT
SALICYLIC ACIDO414PZ4LPZACTIB
MENTHOLL7T10EIP3AIACT
O-CYMEN-5-OLH41B6Q1I9LIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OILVIF565UC2GIACT
POLYQUATERNIUM-10 (125 MPA.S AT 2%)L45WU8S981IACT
HYDROXYPHENYL PROPAMIDOBENZOIC ACID25KRT26H77IACT
PHENOXYETHANOLHIE492ZZ3TIACT
PANTHENOLWV9CM0O67ZIACT
MALTOOLIGOSYL GLUCOSIDEN91S91EFOGIACT
GLYCERINPDC6A3C0OXIACT
BIOTIN6SO6U10H04IACT
PLATYCLADUS ORIENTALIS LEAF32E5V7G32BIACT
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF POWDERIJ67X351P9IACT
FRAGRANCE 135765EM498GW35IACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
PANAX GINSENG ROOTCUQ3A77YXIIACT
GINGERC5529G5JPQIACT

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-dandruffANTI-DANDRUFF SHAMPOOGUANGZHOU YUSONG FINE CHEMICLS Co., Ltd3979fb80-8091-c79e-e063-6394a90ae6182025-07-09WarningsExact identifier
ndc (package): 84558-010-01
ndc (product): 84558-010
ndc11 (package): 84558001001
spl id: 397a1000-1e48-cbf7-e063-6394a90a435d
spl set id: 3979fb80-8091-c79e-e063-6394a90ae618

Reported adverse events (FAERS/openFDA)#

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