Label: PLEO MUC- mucor racemosus capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-1804-1 - Packager: Sanum Kehlbeck GmbH & Co. KG
- Category: HUMAN OTC DRUG LABEL
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 14, 2009
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- SPL UNCLASSIFIED SECTION
- Indications
- INGREDIENTS
- OTHER COMPONENTS
- Tamper Evident
- DOSAGE
- WARNING
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 20 Capsule Carton
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INGREDIENTS AND APPEARANCE
PLEO MUC
mucor racemosus capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-1804 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength mucor racemosus (UNII: 17RH99LQ7G) (mucor racemosus - UNII:17RH99LQ7G) mucor racemosus 4 [HP_X] Inactive Ingredients Ingredient Name Strength lactose (UNII: J2B2A4N98G) 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:60681-1804-1 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 03/01/1996 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)