Label: PLEO MUC- mucor racemosus ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-1806-1 - 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 November 10, 2009
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- SPL UNCLASSIFIED SECTION
- Indications
- DOSAGE
- WARNING
- STORAGE AND HANDLING
- Tamper Evident
- INGREDIENTS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30 g Ointment Carton
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INGREDIENTS AND APPEARANCE
PLEO MUC
mucor racemosus ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-1806 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength mucor racemosus (UNII: 17RH99LQ7G) (mucor racemosus - UNII:17RH99LQ7G) mucor racemosus 3 [hp_X] in 30 g Inactive Ingredients Ingredient Name Strength glyceryl monostearate (UNII: 230OU9XXE4) lactic acid (UNII: 33X04XA5AT) propylene glycol (UNII: 6DC9Q167V3) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-1806-1 1 in 1 CARTON 1 30 g in 1 TUBE 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)