Label: PLEO PEF- candida parapsilosis capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-2502-1 - 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 October 12, 2009
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Indications
- INGREDIENTS
- OTHER COMPONENTS
- Tamper Evident
- DOSAGE
- WARNING
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 20 Capsules Carton
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INGREDIENTS AND APPEARANCE
PLEO PEF
candida parapsilosis capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-2502 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength candida parapsilosis (UNII: 0KZ676D44N) (candida parapsilosis - UNII:0KZ676D44N) candida parapsilosis 4 [HP_X] Inactive Ingredients Ingredient Name Strength lactose (UNII: J2B2A4N98G) hypromellose (UNII: 3NXW29V3WO) Product Characteristics Color YELLOW Score no score Shape CAPSULE Size 19mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-2502-1 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)