FDA.reportPublic FDA data

Shailee Psoriasis Treatment

Manufacturer
Foshan Sugar Max Cosmetics CO.,Ltd
Effective date
2025-11-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:42:18

Label at a glance#

ProductShailee Psoriasis Treatment
Active ingredientSALICYLIC ACID
Label structure7 sections

Indications and uses

Controls flaking, scaling, and itching associated with dandruff.

Dosage and administration

Adults and children aged 12 and over.  Wet hair thoroughly.  Apply shampoo, generously lather, then 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. Children under 12 years old.                Ask a doctor.

Label contents#

Full prescribing information#

Active ingredient                                            Purpose

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 3%                                        Psoriasis and Dandruff Seborrheic Dermatitis

Uses

INDICATIONS & USAGE SECTION

Controls flaking, scaling, and itching associated with dandruff.

Warnings

WARNINGS SECTION

For external use only


Do not use

  • On a damaged or inflamed scalp.
  • If you are allergic to ingredients in this product.

When using this product

  • Avoid contact with the eyes.
  • If contact occurs, rinse the eyes thoroughly with water.

Stop use and ask a doctor if

  • Rash appears.
  • condition worsens or does not improve in 2-4 weeks.

If pregnant or breast-feeding, ask a doctor before use.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children aged 12 and over.
  •  Wet hair thoroughly. 
  • Apply shampoo, generously lather, then 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.
Children under 12 years old.              
  •  Ask a doctor.

Other information

OTHER SAFETY INFORMATION

  • store between 20° – 25°C (68° – 77°F)
  • See bottom panel for lot number and expiration date

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Sodium C-4-16 Olefin Sulfonate, Cocamidopropyl Betaine, PEG-120 Methyl Glucose Dioleate, Polyquaternium-7, Trolamine, Phospholipid EFA, DL Panthenol USP Powder, Vitamin E Acetate, Biotin, Hydrolyzed Keratin, Oxidized Keratin, Rosemary Oil, Tea Tree Oil, Peppermint Oil,Green Tea Extract, Ascorbic Acid, Manuka Honey

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130199284211407GTIN-13: 0199284211407
EAN-13: 0199284211407
GTIN-12: 199284211407
UPC-A: 199284211407
GTIN storage (14 digits): 00199284211407		image_008_updated.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84938-008-01Shailee Psoriasis Treatment1 in 1 CARTONLIQUID11
84938-008-01Shailee Psoriasis Treatment200 mL in 1 BOTTLELIQUID2001

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84938-00884938-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)0L414VCS5YIACT
TROLAMINE9O3K93S3TKIACT
PANTHENOLWV9CM0O67ZIACT
TEA TREE OILVIF565UC2GIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BIOTIN6SO6U10H04IACT
HYDROLYZED SHEEP WOOL KERATIN (200 MW)R6K7AW17SUIACT
ROSEMARY OIL8LGU7VM393IACT
PEPPERMINT OILAV092KU4JHIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ASCORBIC ACIDPQ6CK8PD0RIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
Shailee Psoriasis TreatmentSALICYLIC ACIDFoshan Sugar Max Cosmetics CO.,Ltd02a71ce4-baf5-4231-afd6-21ef0b22e9312025-11-05WarningsExact identifier
ndc (package): 84938-008-01
ndc (product): 84938-008
ndc11 (package): 84938000801
spl id: 42de3b25-692d-eaff-e063-6294a90a0d21
spl set id: 02a71ce4-baf5-4231-afd6-21ef0b22e931

Reported adverse events (FAERS/openFDA)#

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