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natralia (LaCorium Health International Pty Ltd)

Available Formats

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

Complete natralia Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • ACTIVE INGREDIENT

    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.

    Stop use and ask a doctor if
    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days.

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

    Keep out of the 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
    • Suitable for use on children 2 years of age and older

  • Other Information

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


  • Inactive Ingredients

    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?

    Call Toll Free 1-877-687-2542

    usainfo@natralia.com

    www.natralia.com


  • PRINCIPAL DISPLAY PANEL - 56 g Tube Carton

    NDC: 43251-2241-1

    natraliaâ„¢
    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

  • 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)
    Establishment
    Name Address ID/FEI Business Operations
    Denison Pharmaceuticals LLC 001207208 MANUFACTURE(43251-2241) , PACK(43251-2241) , ANALYSIS(43251-2241) , LABEL(43251-2241)