FDA.reportPublic FDA data

Neoketramin Antifungal Dandruff Seborrheic Dermatitis Psoriasis Treatment

Manufacturer
Rida LLC
Effective date
2025-03-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:56:51

Label at a glance#

ProductNeoketramin Antifungal Dandruff Seborrheic Dermatitis Psoriasis Treatment
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

Relieves and helps prevent recurrence of scalp: irritation itching redness flaking scaling due to psoriasis and seborrheic dermatitis

Dosage and administration

 Adults and children aged 12 and over  wet hair thoroughly Apply shampoo, generously lather, then rinse thoroughly. Repeate 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

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 3%

Purpose

OTC - PURPOSE SECTION

Psoriasis Dandruff
Seborrheic Dermatitis

Uses

INDICATIONS & USAGE SECTION

Relieves and helps prevent recurrence of scalp:

  • irritation
  • itching
  • redness
  • flaking
  • scaling due to psoriasis and seborrheic dermatitis

Directions

DOSAGE & ADMINISTRATION SECTION

 Adults and children aged 12 and over
  •  wet hair thoroughly
  • Apply shampoo, generously lather, then rinse thoroughly. Repeate
  • 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

SPL UNCLASSIFIED SECTION

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

Warnings

WARNINGS SECTION

For external use only
Do not use

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

When using this product

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

Stop use and ask a doctor if:

  • Rash appears
  • Condition worsen 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ascorbic Acid, Cocamidopropyl Betaine, DL Panthenol USP Powder, Green Tea Extract, Linolemidopropyl PG-Dimonium Chloride Phosphate, PEG-120 Methyl Glucose Dioleate, Polyquaternium-7, Propylene Glycol, Puried Water, Sodium C-14-16 Olefin Sulfonate, Tea Tree Oil, Trolamine, Vitamin E Acetate

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83004-019-012025-08-20C16284748780-13b156c62-2874-fb37-e063-e6dba90a4e0761761914-3bb5-4034-a014-82500949672c
83004-019-012025-07-29C16284748780-13b156c62-2874-fb37-e063-e6dba90a4e0761761914-3bb5-4034-a014-82500949672c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83004-019-01Neoketramin Antifungal Dandruff Seborrheic Dermatitis Psoriasis Treatment1 in 1 CARTONLIQUID11
83004-019-01Neoketramin Antifungal Dandruff Seborrheic Dermatitis Psoriasis Treatment200 mL in 1 TUBELIQUID2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83004-019NEOKETRAMIN ANTIFUNGAL DANDRUFF SEBORRHEIC DERMATITIS PSORIASIS TREATMENT (SALICYLIC ACID) LIQUID [RIDA LLC]12 package rows20250309_61761914-3bb5-4034-a014-82500949672c.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83004-01983004-019-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TEA TREE OILVIF565UC2GIACT
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
58b7068a-ce86-bc7c-e063-6394a90ae86561761914-3bb5-4034-a014-82500949672c2026-08-10WarningsExact identifier
spl set id: 61761914-3bb5-4034-a014-82500949672c

Reported adverse events (FAERS/openFDA)#

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