Label: PLEO LARI- laricifomes officinalis fruiting body solution/ drops

  • 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 August 1, 2011

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  • SPL UNCLASSIFIED SECTION

    Homeopathic Analgesic Medicine

    0.34 fl oz
    (10 mL)

  • Indications

    For temporary relief of primary chronic polyarthritis symptoms.

  • INGREDIENTS

    10 mL Laricifomes officinalis e mycelio 5X.

  • INACTIVE INGREDIENT

    Purified Water

  • Tamper Evident

    Use this product only if tamper-evident strip at base of bottle cap is intact.

  • DOSAGE

    5–10 drops, once daily, before mealtime.

  • WARNING

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

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

  • STORAGE AND HANDLING

    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. 02/2003

  • PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton

    Pleo™ –Lari
    DROPS 5X
    Homeopathic
    Analgesic
    Medicine

    Indications: For
    temporary relief
    of primary
    chronic
    polyarthritis
    symptoms.

    0.34 fl oz
    (10 mL)

    Principal Display Panel - 10 mL Bottle Carton
  • INGREDIENTS AND APPEARANCE
    PLEO LARI 
    laricifomes officinalis fruiting body solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60681-1301
    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 body5 [hp_X]  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60681-1301-11 in 1 CARTON
    110 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED HOMEOPATHIC03/19/1996
    Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)
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