FDA.reportPublic FDA data

Grahams Natural Psoriasis and Dermatitis

Manufacturer
Grahams Natural Alternatives Pty Ltd
Effective date
2015-09-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:43:29

Label at a glance#

ProductGrahams Natural Psoriasis and Dermatitis
Active ingredientSALICYLIC ACID
Label structure10 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Purpose

Psoriasis/Seborrheic Dermatitis

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Salicylic Acid 2%

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

Uses/Indications

For the relief of the symptoms of psoriasis and/or seborrheic dermatitis

DOSAGE & ADMINISTRATION SECTION

Directions

Apply to affected area 1-4 times daily or as directed by a doctor

WARNINGS SECTION

Warnings for external use only

If contact occurs, rinse eyes thoroughly with water

If condition worsens or does not improve after regular use of this product as directed, consult a doctor.

If condition covers a large area of the body, consult your doctor before using this product.

DESCRIPTION SECTION

Grahams Natural Psoriasis & Dermatitis Cream

Grahams Natural Psoriasis and Dermatitis Cream is a unique formulation using the soothing benefits of calendula, gotu kola and propolis along with the healing qualities of manuka honey.

steroid and fragrance free

Nature at its Best

OTC - QUESTIONS SECTION

Other Information

Store below 86F or 30C

For best results use with Grahams Natural Bath Oil

Questions  www.itchy.net.au

Made in Australia

Grahams Natural Alternatives Pty Ltd

7 Palings Crt, Nerang, QLD 4211 Australia

INACTIVE INGREDIENT SECTION

Inactive Ingredients

aqua, cetostearyl alcohol, calendula officinalis, centella asiatica, manuka honey, propolis, cetomacrogol, phenoxyethanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
317152salicylic acid 2 % Topical CreamPSN2
317152salicylic acid 20 MG/ML Topical CreamSCD2
317152salicylic acid 2 % Topical CreamSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42387-200-012020-01-31C16284748780-19d75b9d0-fdf6-f424-e053-dadaa90a57ce4b69a66c-3490-4e26-b8f7-7c59f0c8f244

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42387-200-01Grahams Natural Psoriasis and Dermatitis57 g in 1 PACKAGECREAM572

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42387-200GRAHAMS NATURAL PSORIASIS AND DERMATITIS (SALICYLIC ACID) CREAM [GRAHAMS NATURAL ALTERNATIVES PTY LTD]2Legacy NDC, 1 package rows20150903_4b69a66c-3490-4e26-b8f7-7c59f0c8f244.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ2
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ2
CALENDULA OFFICINALIS FLOWERINACTIVE INGREDIENTP0M7O4Y7YD2
CENTELLA ASIATICAINACTIVE INGREDIENT7M867G6T1U2
CETETH-20INACTIVE INGREDIENTI835H2IHHX2
CETOSTEARYL ALCOHOLINACTIVE INGREDIENT2DMT128M1S2
HONEYINACTIVE INGREDIENTY9H1V576FH2
PHENOXYETHANOLINACTIVE INGREDIENTHIE492ZZ3T2
PROPOLIS WAXINACTIVE INGREDIENT6Y8XYV2NOF2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42387-20042387-200-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
CENTELLA ASIATICA7M867G6T1UIACT
HONEYY9H1V576FHIACT
PROPOLIS WAX6Y8XYV2NOFIACT
CETETH-20I835H2IHHXIACT
PHENOXYETHANOLHIE492ZZ3TIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 19 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TAEROSOL, FOAM / TOPICAL72 mgExact identifier — unii candidate
6 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TAEROSOL / TOPICAL1.05 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SLOTION / TOPICAL3627 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1STABLET, EXTENDED RELEASE / ORAL800 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SSPRAY / TOPICAL1 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TCREAM / TOPICAL57 mgExact identifier — unii candidate
6 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TCREAM, AUGMENTED / TOPICAL10 mgExact identifier — unii candidate
6 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SCAPSULE, EXTENDED RELEASE / ORAL9.43 mgExact identifier — unii candidate
9 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii candidate
6 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SCREAM / TOPICAL1428 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETETH-20CETETH-20I835H2IHHXLOTION / TOPICAL2 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SAEROSOL, FOAM / TOPICAL21 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETETH-20CETETH-20I835H2IHHXTAMPON / VAGINALNAExact identifier — unii candidate
4 equally ranked IID candidates
CETETH-20CETETH-20I835H2IHHXCREAM / TOPICAL429 mgExact identifier — unii candidate
4 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SOINTMENT / TOPICAL1.2 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SSUPPOSITORY / VAGINALNAExact identifier — unii candidate
9 equally ranked IID candidates
CETETH-20CETETH-20I835H2IHHXSOLUTION / TOPICAL2 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SCREAM / VAGINAL6 mgExact identifier — unii candidate
9 equally ranked IID candidates

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
a702b975-90f2-4224-8030-5a425388cd444b69a66c-3490-4e26-b8f7-7c59f0c8f2442015-09-03WarningsExact identifier
spl id: a702b975-90f2-4224-8030-5a425388cd44
spl set id: 4b69a66c-3490-4e26-b8f7-7c59f0c8f244

Reported adverse events (FAERS/openFDA)#

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