Flexitol NATURALS ® ECZEMA & PSORIASIS CREAM

Manufacturer
LaCorium Health International Pty Ltd
Effective date
2012-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:03:31

Label at a glance#

ProductFlexitol Naturals 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 For best results use together with FLEXITOL NATURALS Eczema & Psoriasis Wash.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children

OTC - STOP USE SECTION

  • If condition worsens or does not improve after regular use of this product as directed or if local irritation or rash occurs, discontinue use and consult a physician.

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
  • For best results use together with FLEXITOL NATURALS Eczema & Psoriasis Wash.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cetearyl Alcohol, Paraffin, Zinc Oxide, Paraffin Oil, Lavender Oil, Ceteareth-20, Licorice (Glycyrrhiza Glabra) Extract, Avocado Oil, Chamomile Oil, Diazolidinyl Urea, Phenoxyethanol, Evening Primrose Oil, Tocopheryl Acetate, Aloe Vera Gel

Questions or comments?

OTC - QUESTIONS SECTION

Call Toll Free 1-866-478-3338
usainfo@flexitol.com
www.flexitol.com

PRINCIPAL DISPLAY PANEL - 56 g Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NON
STEROIDAL

Flexitol
NATURALS
®

Trust Flexitol . . .

ECZEMA
& PSORIASIS
CREAM

. . . it really works!

Before
After

For the Relief of
Skin Irritation, Itching,
Flaking & Dryness

Contains 0.2% Ethanol w/w

Net Wt 2 oz (56 g)

PRINCIPAL DISPLAY PANEL - 56 g Carton
PRINCIPAL DISPLAY PANEL - 56 g Carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43251-2231-12019-11-13C16284748780-197449f38-c84b-f6ea-e053-dbdaa90aa703Flexitol NATURALS ® ECZEMA & PSORIASIS CREAM
43251-2231-22019-11-13C16284748780-197449f38-c84b-f6ea-e053-dbdaa90aa703Flexitol NATURALS ® ECZEMA & PSORIASIS CREAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43251-2231-1Flexitol Naturals Eczema and Psoriasis1 in 1 CARTONCREAM12
43251-2231-1Flexitol Naturals Eczema and Psoriasis56 g in 1 TUBECREAM562
43251-2231-2Flexitol Naturals Eczema and Psoriasis1 g in 1 PACKETCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43251-2231FLEXITOL NATURALS ECZEMA AND PSORIASIS (SODIUM BORATE, GRAPHITE, POTASSIUM SULFATE, AND SODIUM CHLORIDE) CREAM [LACORIUM HEALTH INTERNATIONAL PTY LTD]2Legacy NDC, 3 package rows20120124_1cc64c25-d55e-458d-a8c0-77e2997c0369.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GraphiteACTIVE INGREDIENT4QQN74LH4O2
Potassium SulfateACTIVE INGREDIENT1K573LC5TV2
Sodium BorateACTIVE INGREDIENT91MBZ8H3QO2
Sodium ChlorideACTIVE INGREDIENT451W47IQ8X2
GraphiteACTIVE MOIETY4QQN74LH4O2
Potassium CationACTIVE MOIETY295O53K1522
Sodium CationACTIVE MOIETYLYR4M0NH372
Avocado OilINACTIVE INGREDIENT6VNO72PFC12
Caprylyl GlycolINACTIVE INGREDIENT00YIU5438U2
Cetearyl GlucosideINACTIVE INGREDIENT09FUA47KNA2
Cetostearyl AlcoholINACTIVE INGREDIENT2DMT128M1S2
Chamaemelum Nobile Flower OilINACTIVE INGREDIENTUB275878392
Cocoa ButterINACTIVE INGREDIENT512OYT1CRR2
Evening Primrose OilINACTIVE INGREDIENT3Q9L08K71N2
Glycyrrhiza GlabraINACTIVE INGREDIENT2788Z9758H2
Lavandula Angustifolia FlowerINACTIVE INGREDIENT19AH1RAF4M2
PhenoxyethanolINACTIVE INGREDIENTHIE492ZZ3T2
Shea ButterINACTIVE INGREDIENTK49155WL9Y2
Sorbic AcidINACTIVE INGREDIENTX045WJ989B2
WaterINACTIVE INGREDIENT059QF0KO0R2
Zinc OxideINACTIVE INGREDIENTSOI2LOH54Z2

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43251-223143251-2231-1, 43251-2231-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

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 OXIDESOI2LOH54ZSUPPOSITORY / RECTAL375 mgExact identifier — unii candidate
6 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BCREAM / TOPICAL14 mgExact identifier — unii candidate
19 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii candidate
6 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET / SUBLINGUAL0.16 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, FILM COATED / ORAL5 mgExact identifier — unii candidate
19 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SLOTION / TOPICAL3627 mgExact identifier — unii candidate
9 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM, AUGMENTED / TOPICAL10 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM / TOPICAL57 mgExact identifier — unii candidate
6 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BSOLUTION/ DROPS / OPHTHALMIC0.2 %w/vExact identifier — unii candidate
19 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SCAPSULE, EXTENDED RELEASE / ORAL9.43 mgExact identifier — unii candidate
9 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BOINTMENT / TOPICAL0.1 %w/wExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, DELAYED RELEASE / ORAL0.03 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 ACIDX045WJ989BTABLET / ORAL10 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BSOLUTION / ORAL80 mgExact identifier — unii candidate
19 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SCREAM / VAGINAL6 mgExact identifier — unii candidate
9 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BSOLUTION / OPHTHALMIC0.2 %w/vExact identifier — unii candidate
19 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SOINTMENT / TOPICAL1.2 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL / TOPICAL1.05 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, CHEWABLE / ORALNAExact identifier — unii candidate
19 equally ranked IID candidates
Cocoa ButterCOCOA BUTTER512OYT1CRRSUPPOSITORY / RECTAL2280 mgExact identifier — unii candidate
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SSPRAY / TOPICAL1 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SAEROSOL, FOAM / TOPICAL21 mgExact identifier — unii candidate
9 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BAEROSOL, FOAM / TOPICAL6 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BTABLET, COATED / ORAL1 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BCONCENTRATE / ORAL1 mgExact identifier — unii candidate
19 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SSUPPOSITORY / VAGINALNAExact identifier — unii candidate
9 equally ranked IID candidates
Zinc OxideZINC OXIDESOI2LOH54ZSOLUTION / RESPIRATORY (INHALATION)3.11 %w/vExact identifier — unii candidate
6 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1SCREAM / TOPICAL1428 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 ACIDX045WJ989BSUSPENSION / ORAL40 mgExact identifier — unii candidate
19 equally ranked IID candidates
Cetostearyl AlcoholCETOSTEARYL ALCOHOL2DMT128M1STABLET, EXTENDED RELEASE / ORAL800 mgExact identifier — unii candidate
9 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
Sorbic AcidSORBIC ACIDX045WJ989BGEL / TOPICAL2 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BLOTION / TOPICAL4 mgExact identifier — unii candidate
19 equally ranked IID candidates
Sorbic AcidSORBIC ACIDX045WJ989BEMULSION / OPHTHALMIC1 mgExact identifier — unii candidate
19 equally ranked IID candidates
Zinc OxideZINC OXIDESOI2LOH54ZSOLUTION / INTRAVENOUS3.11 %w/vExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL, FOAM / TOPICAL72 mgExact identifier — unii candidate
6 equally ranked IID candidates
Zinc OxideZINC OXIDESOI2LOH54ZLOTION / TOPICAL16 %w/wExact 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
f268a8f9-84db-453a-8e1f-1b8c692724d21cc64c25-d55e-458d-a8c0-77e2997c03692012-01-20WarningsExact identifier
spl id: f268a8f9-84db-453a-8e1f-1b8c692724d2
spl set id: 1cc64c25-d55e-458d-a8c0-77e2997c0369

Reported adverse events (FAERS/openFDA)#

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