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natralia (LaCorium Health International Pty Ltd)

Available Formats

Dosage Form Package Information Links
CREAM 1 TUBE in 1 CARTON (43251-2241-1) > 56 g in 1 TUBE Label Information
CREAM 1 g in 1 PACKET (43251-2241-2) Label Information

Complete natralia Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • ACTIVE INGREDIENT

    *
    • 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.
    Active Ingredients Purpose
    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

    • 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

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

    • Keep out of reach of children

  • 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

  • Other Information

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

  • Inactive Ingredients

    Water, Cetearyl Alcohol, Capric/Caprylic Triglycerides, Zinc Oxide, Lavandula Angustifolia (Lavender) Oil, Glycyrrhiza Glabra (Licorice) Root Extract, Cetearyl Glucoside, Persea Gratissima (Avocado) Oil, Theobroma Cacao Butter, Butyrospermum Parkii (Shea Butter), Caprylyl Glycol (and) Sorbic Acid (and) Phenoxyethanol, Methyl Glucose Sesquistearate, Anthemis Nobilis (Chamomile) Oil, Oenothera Biennis (Evening Primrose) Oil, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice


  • Questions or Comments?

    Call Toll Free 1-877-687-2542
    usainfo@natralia.com.au
    www.natralia.com.au/usa


  • PRINCIPAL DISPLAY PANEL - 56 g Tube Carton

    NDC: 43251-2241-1

    natraliaâ„¢
    NATURALLY AUSTRALIAN

    Eczema &
    Psoriasis
    Cream

    RASH RELIEF

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

    CORTISONE
    FREE

    SUITABLE FOR CHILDREN

    Contains 0.2% ethanol w/w

    Net Wt 2 oz (56g)

    Principal Display Panel - 56 g Tube Carton

  • INGREDIENTS AND APPEARANCE
    NATRALIA   ECZEMA AND PSORIASIS
    sodium borate, graphite, potassium sulfate, and sodium chloride cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43251-2241
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Sodium Borate (UNII: 91MBZ8H3QO) (Borate ion - UNII:44OAE30D22) Sodium Borate 20 [hp_X]  in 1 g
    Graphite (UNII: 4QQN74LH4O) (Graphite - UNII:4QQN74LH4O) Graphite 6 [hp_X]  in 1 g
    Potassium Sulfate (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) Potassium Sulfate 3 [hp_X]  in 1 g
    Sodium Chloride (UNII: 451W47IQ8X) (Sodium Cation - UNII:LYR4M0NH37) Sodium Chloride 12 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    Cetostearyl Alcohol (UNII: 2DMT128M1S)  
    Zinc Oxide (UNII: SOI2LOH54Z)  
    LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    Glycyrrhiza Glabra (UNII: 2788Z9758H)  
    Cetearyl Glucoside (UNII: 09FUA47KNA)  
    Avocado Oil (UNII: 6VNO72PFC1)  
    Cocoa Butter (UNII: 512OYT1CRR)  
    Shea Butter (UNII: K49155WL9Y)  
    Caprylyl Glycol (UNII: 00YIU5438U)  
    Sorbic Acid (UNII: X045WJ989B)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Chamaemelum Nobile Flower Oil (UNII: UB27587839)  
    Evening Primrose Oil (UNII: 3Q9L08K71N)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43251-2241-1 1 in 1 CARTON 03/01/2009
    1 56 g in 1 TUBE; Type 0: Not a Combination Product
    2 NDC:43251-2241-2 1 g in 1 PACKET; Type 0: Not a Combination Product 03/01/2009
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved homeopathic 03/01/2009
    Labeler - LaCorium Health USA Inc. (111254392)
    Establishment
    Name Address ID/FEI Business Operations
    Ross Cosmetics Australia Pty. Ltd. 753529114 MANUFACTURE(43251-2241) , PACK(43251-2241) , ANALYSIS(43251-2241)