Label: PLEO UT S- mycobacterium phlei solution/ drops
-
Contains inactivated NDC Code(s)
NDC Code(s): 60681-5401-2 - 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 March 9, 2012
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PURPOSE
- Indications
- ACTIVE INGREDIENT
- Tamper Evident
- DOSAGE
-
WARNING
If symptoms persist more than a few days, contact a licensed practitioner. As with other drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before using this product.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 5 mL Carton
-
INGREDIENTS AND APPEARANCE
PLEO UT S
mycobacterium phlei solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-5401 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength mycobacterium phlei (UNII: T67520T45F) (mycobacterium phlei - UNII:T67520T45F) mycobacterium phlei 6 [hp_X] in 5 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-5401-2 1 in 1 CARTON 1 5 mL in 1 BOTTLE, DROPPER 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)