FDA.reportPublic FDA data

natralia™ NATURALLY AUSTRALIAN eczema & psoriasis cream

Manufacturer
LaCorium Health USA Inc. | Ross Cosmetics Australia Pty. Ltd. | Denison Pharmaceuticals LLC
Effective date
2020-12-15
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 23:00:43

Label at a glance#

Productnatralia eczema and psoriasis
Active ingredientSodium Borate, Graphite, Potassium Sulfate, Sodium Chloride
Label structure9 sections

Indications and uses

Use on affected areas for relief of itching, irritation, redness, flaking and scaling associated with Eczema & Psoriasis.

Dosage and administration

Apply to affected skin 2-3 times daily Smooth in gently The smallest effective dose should be used Patch test recommended on sensitive skin Suitable for use on children 2 years of age and older

Storage and handling

Store between 50°- 86°F in a dry place

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active IngredientsPurpose
Borax (20 X H.P.U.S.0.2%)* †E & P R
Graphites (6 X H.P.U.S.0.2%)* †E & P R
Kalium Sulphuricum (3 X H.P.U.S. 0.2%)* †E & P R
Natrum Muriaticum (12 X H.P.U.S. 0.2%)* †E & P R

* The letters H.P.U.S. indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

† The letters E & P R indicate Eczema & Psoriasis Relief.

Uses

INDICATIONS & USAGE SECTION

Use on affected areas for relief of itching, irritation, redness, flaking and scaling associated with Eczema & Psoriasis.

Warnings

WARNINGS SECTION

For external use only.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days.

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes
  • If contact occurs, rinse eyes thoroughly with water.
  • Do not use on broken skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to affected skin 2-3 times daily
  • Smooth in gently
  • The smallest effective dose should be used
  • Patch test recommended on sensitive skin
  • Suitable for use on children 2 years of age and older

Other Information

STORAGE AND HANDLING SECTION

Store between 50°- 86°F in a dry place

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Anthemis Nobilis (Chamomile) Oil, Butyrospermum Parkii (Shea) Butter, Capric/Caprylic Triglyceride, Caprylyl Glycol, Cetearyl Alcohol, Ceteareth-20, Glycyrrhiza Glabra (Licorice) Root Extract, Lavandula Angustifolia (Lavender) Oil, Oenothera Biennis (Evening Primrose) Oil, Persea Gratissima (Avocado) Oil, Phenoxyethanol, Sorbic Acid, Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate, Water, Zinc Oxide

Questions or Comments?

OTC - QUESTIONS SECTION

Call Toll Free 1-877-687-2542

usainfo@natralia.com

www.natralia.com

PRINCIPAL DISPLAY PANEL - 56 g Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43251-2241-1

natralia™
NATURALLY AUSTRALIAN

Eczema &
Psoriasis
Cream

RASH RELIEF

BEFORE

AFTER

  • Relieves rash,
    irritation, itching
    and redness
  • Free from
    cortisone, coal
    and pine tar

Proud Supporter
eczema
association
australasia
eaa

SUITABLE FOR CHILDREN

Homeopathic

Net Wt 2 oz (56g)

Principal Display Panel - 56 g Tube Carton
Principal Display Panel - 56 g Tube Carton

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GraphiteACTIVE INGREDIENT4QQN74LH4O4
Potassium SulfateACTIVE INGREDIENT1K573LC5TV4
Sodium BorateACTIVE INGREDIENT91MBZ8H3QO4
Sodium ChlorideACTIVE INGREDIENT451W47IQ8X4
Borate ionACTIVE MOIETY44OAE30D224
GraphiteACTIVE MOIETY4QQN74LH4O4
Sodium CationACTIVE MOIETYLYR4M0NH374
SULFATE IONACTIVE MOIETY7IS9N8KPMG4
Aloe Vera LeafINACTIVE INGREDIENTZY81Z83H0X4
Avocado OilINACTIVE INGREDIENT6VNO72PFC14
Caprylyl GlycolINACTIVE INGREDIENT00YIU5438U4
Cetearyl GlucosideINACTIVE INGREDIENT09FUA47KNA4
Cetostearyl AlcoholINACTIVE INGREDIENT2DMT128M1S4
Chamaemelum Nobile Flower OilINACTIVE INGREDIENTUB275878394
Cocoa ButterINACTIVE INGREDIENT512OYT1CRR4
Evening Primrose OilINACTIVE INGREDIENT3Q9L08K71N4
Glycyrrhiza GlabraINACTIVE INGREDIENT2788Z9758H4
Lavandula Angustifolia FlowerINACTIVE INGREDIENT19AH1RAF4M4
PhenoxyethanolINACTIVE INGREDIENTHIE492ZZ3T4
Shea ButterINACTIVE INGREDIENTK49155WL9Y4
Sorbic AcidINACTIVE INGREDIENTX045WJ989B4
WaterINACTIVE INGREDIENT059QF0KO0R4
Zinc OxideINACTIVE INGREDIENTSOI2LOH54Z4

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43251-224143251-2241-1, 43251-2241-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
Sodium Borate91MBZ8H3QOACTIB
Graphite4QQN74LH4OACTIB
Potassium Sulfate1K573LC5TVACTIB
Sodium Chloride451W47IQ8XACTIB
Water059QF0KO0RIACT
Cetostearyl Alcohol2DMT128M1SIACT
Zinc OxideSOI2LOH54ZIACT
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER19AH1RAF4MIACT
Glycyrrhiza Glabra2788Z9758HIACT
Cetearyl Glucoside09FUA47KNAIACT
Avocado Oil6VNO72PFC1IACT
Cocoa Butter512OYT1CRRIACT
Shea ButterK49155WL9YIACT
Caprylyl Glycol00YIU5438UIACT
Sorbic AcidX045WJ989BIACT
PhenoxyethanolHIE492ZZ3TIACT
Chamaemelum Nobile Flower OilUB27587839IACT
Evening Primrose Oil3Q9L08K71NIACT
Aloe Vera LeafZY81Z83H0XIACT

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 · 42 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Zinc OxideZINC OXIDESOI2LOH54ZSOLUTION / INTRAVENOUS3.11 %w/vExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM / TOPICAL57 mgExact identifier — unii candidate
6 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SSPRAY / TOPICAL1 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SOINTMENT / TOPICAL1.2 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii candidate
6 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, DELAYED RELEASE / ORAL0.03 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET / SUBLINGUAL0.16 mgExact identifier — unii candidate
19 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
Cocoa ButterCOCOA BUTTER512OYT1CRRSUPPOSITORY / RECTAL2280 mgExact identifier — unii candidate
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SCAPSULE, EXTENDED RELEASE / ORAL9.43 mgExact identifier — unii candidate
9 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BSUSPENSION / ORAL40 mgExact identifier — unii candidate
19 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SCREAM / VAGINAL6 mgExact identifier — unii candidate
9 equally ranked IID candidates
Zinc OxideZINC OXIDESOI2LOH54ZINJECTION / SUBCUTANEOUS0.02 %w/vExact identifier — unii candidate
6 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BSYRUP / ORAL80 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BGEL / TOPICAL2 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BCONCENTRATE / ORAL1 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, FILM COATED, EXTENDED RELEASE / ORAL1 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BSOLUTION / OPHTHALMIC0.2 %w/vExact identifier — unii candidate
19 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL / TOPICAL1.05 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SAEROSOL, FOAM / TOPICAL21 mgExact identifier — unii candidate
9 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SSUPPOSITORY / VAGINALNAExact identifier — unii candidate
9 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, FILM COATED / ORAL5 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BEMULSION / OPHTHALMIC1 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BSOLUTION / ORAL80 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BOINTMENT / TOPICAL0.1 %w/wExact identifier — unii candidate
19 equally ranked IID candidates
Zinc OxideZINC OXIDESOI2LOH54ZLOTION / TOPICAL16 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL, FOAM / TOPICAL72 mgExact identifier — unii candidate
6 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BAEROSOL, FOAM / TOPICAL6 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BCREAM / TOPICAL14 mgExact identifier — unii candidate
19 equally ranked IID candidates
Zinc OxideZINC OXIDESOI2LOH54ZINJECTION, SUSPENSION / SUBCUTANEOUSNAExact identifier — unii candidate
6 equally ranked IID candidates
Shea ButterSHEA BUTTERK49155WL9YLOTION / TOPICAL2340 mgExact identifier — unii candidate
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1STABLET, EXTENDED RELEASE / ORAL800 mgExact identifier — unii candidate
9 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM, AUGMENTED / TOPICAL10 mgExact identifier — unii candidate
6 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SCREAM / TOPICAL1428 mgExact identifier — unii candidate
9 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BSOLUTION/ DROPS / OPHTHALMIC0.2 %w/vExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BLOTION / TOPICAL4 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, COATED / ORAL1 mgExact identifier — unii candidate
19 equally ranked IID candidates
Zinc OxideZINC OXIDESOI2LOH54ZSOLUTION / RESPIRATORY (INHALATION)3.11 %w/vExact identifier — unii candidate
6 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SLOTION / TOPICAL3627 mgExact identifier — unii candidate
9 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET / ORAL10 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, CHEWABLE / ORALNAExact identifier — unii candidate
19 equally ranked IID candidates
Zinc OxideZINC OXIDESOI2LOH54ZSUPPOSITORY / RECTAL375 mgExact identifier — unii candidate
6 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
8178bf6e-c7d4-4f2d-83ef-0dba183ce28190705b9c-4f2b-48da-84de-711dd824595e2020-12-15WarningsExact identifier
spl id: 8178bf6e-c7d4-4f2d-83ef-0dba183ce281
spl set id: 90705b9c-4f2b-48da-84de-711dd824595e

Reported adverse events (FAERS/openFDA)#

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