Label: PLEO LARI- laricifomes officinalis fruiting body capsule

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated January 6, 2010

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Homeopathic Arthritis Pain Relief Medicine

    20 CAPSULES

  • Indications

    For temporary relief of pain associated with arthritis.

  • INGREDIENTS

    1 capsule contains 330 mg Laricifomes officinalis e mycelio 4X in a base of lactose.

  • Tamper Evident

    Do not use this product if shrink-wrap is missing from the carton or the imprinted blister foil is broken.

  • DOSAGE

    1–3 capsules daily, either before breakfast or at bedtime.

  • WARNING

    If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before taking this product.

    Keep this and all medications out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

    Protect from light and heat.

  • SPL UNCLASSIFIED SECTION

    Made in Germany

    Distributed by:
    SANUM USA Corp.
    1465 Slater Road
    Ferndale, WA 98248

    Manufactured By:
    Sanum-Kehlbeck
    GmbH & Co. KG

    Rev. 07/2004

  • PRINCIPAL DISPLAY PANEL - 20 Capsule Carton

    Pleo™ Lari
    CAPSULES 4X

    Homeopathic Arthritis
    Pain Relief Medicine

    Indications: For temporary
    relief of pain associated
    with arthritis.

    20 CAPSULES

    PRINCIPAL DISPLAY PANEL - Capsule Carton
  • INGREDIENTS AND APPEARANCE
    PLEO LARI 
    laricifomes officinalis fruiting body capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60681-1302
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    laricifomes officinalis fruiting body (UNII: 7IFM8431X3) (laricifomes officinalis fruiting body - UNII:7IFM8431X3) laricifomes officinalis fruiting body4 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    lactose (UNII: J2B2A4N98G)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeCAPSULESize19mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60681-1302-11 in 1 CARTON
    120 in 1 BLISTER PACK
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved homeopathic03/19/1996
    Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)