FLEXITOL NATURALS ECZEMA AND PSORIASIS - sodium borate, graphite, potassium sulfate and sodium chloride cream 
Laderma Trading Pty Ltd

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Flexitol
NATURALS ®
ECZEMA
& PSORIASIS
CREAM

Drug Facts

Active ingredients	Purpose
* 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.
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

Uses

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

Warnings

• For External Use Only
   
• Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water

• Keep out of reach of children

• 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

• 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

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

Inactive ingredients

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?

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

PRINCIPAL DISPLAY PANEL - 56 g Carton

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)

FLEXITOL NATURALS ECZEMA AND PSORIASIS  sodium borate, graphite, potassium sulfate, and sodium chloride   cream

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 43251-2231 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium Borate (Sodium Cation) Sodium Borate 20 [hp_X]  in 1 g Graphite (Graphite) Graphite 6 [hp_X]  in 1 g Potassium Sulfate (Potassium Cation) Potassium Sulfate 3 [hp_X]  in 1 g Sodium Chloride (Sodium Cation) Sodium Chloride 12 [hp_X]  in 1 g

Inactive Ingredients Ingredient Name Strength Zinc Oxide   Cetostearyl Alcohol   Lavandula Angustifolia Flower   Cocoa Butter   Glycyrrhiza Glabra   Avocado Oil   Shea Butter   Cetearyl Glucoside   Caprylyl Glycol   Sorbic Acid   Phenoxyethanol   Chamaemelum Nobile Flower Oil   Evening Primrose Oil   Water

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 43251-2231-1 1 TUBE In 1 CARTON contains a TUBE 1 56 g In 1 TUBE This package is contained within the CARTON (43251-2231-1) 2 43251-2231-2 1 g In 1 PACKET None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED HOMEOPATHIC		01/03/2009

Labeler - Laderma Trading Pty Ltd (758651624)

Revised: 05/2011Laderma Trading Pty Ltd