Label: PLEO SAN MYC- mycobacterium bovis solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-1204-1 - 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 November 9, 2011
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- Official Label (Printer Friendly)
- PURPOSE
- Indications
- INGREDIENTS
- Tamper Evident
- DOSAGE
- WARNING
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 10 mL Carton
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INGREDIENTS AND APPEARANCE
PLEO SAN MYC
mycobacterium bovis solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-1204 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength mycobacterium bovis (UNII: XZQ806VFEO) (mycobacterium bovis - UNII:XZQ806VFEO) mycobacterium bovis 6 [hp_X] in 10 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-1204-1 1 in 1 CARTON 1 10 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 09/19/1997 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)