Label: PLEO LARI- laricifomes officinalis fruiting body capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-1302-1 - Packager: Sanum Kehlbeck GmbH & Co. KG
- 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.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Indications
- INGREDIENTS
- Tamper Evident
- DOSAGE
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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.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 20 Capsule Carton
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INGREDIENTS AND APPEARANCE
PLEO LARI
laricifomes officinalis fruiting body capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-1302 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength laricifomes officinalis fruiting body (UNII: 7IFM8431X3) (laricifomes officinalis fruiting body - UNII:7IFM8431X3) laricifomes officinalis fruiting body 4 [hp_X] Inactive Ingredients Ingredient Name Strength lactose (UNII: J2B2A4N98G) Product Characteristics Color WHITE Score no score Shape CAPSULE Size 19mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-1302-1 1 in 1 CARTON 1 20 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 03/19/1996 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)