Label: PLEO MUC EX- mucor racemosus immunoserum rabbit liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-1905-1, 60681-1905-2 - 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 February 3, 2010
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- INDICATIONS
- DIRECTIONS FOR USE
- DOSAGE
- INGREDIENTS
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WARNING
If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before using this product.
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 1 mL Vial Carton
1905-1
Pleo™ Muc EX
PORTABLE SIPS 6XOral Homeopathic Medicine
INDICATIONS: For elimination and di-
uretic action.DIRECTIONS FOR USE: Snap off top
portion of sipping container. Insert glass
sipping straw.DOSAGE: 1 SIP, once weekly, after use
of Pleo™ Muc.INGREDIENTS: 1 mL contains Mucor
racemosus Anti chrondrite serum 6X, in a
base of purified saline solution.convenient, disposable
single dose containers10 doses, each 1 mL
(.03 fl oz)Rev. 8/99
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INGREDIENTS AND APPEARANCE
PLEO MUC EX
mucor racemosus immunoserum rabbit liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-1905 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Mucor racemosus immunoserum rabbit (UNII: 83EHL3RVHX) (Mucor racemosus immunoserum rabbit - UNII:83EHL3RVHX) Mucor racemosus immunoserum rabbit 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength sodium chloride (UNII: 451W47IQ8X) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-1905-1 10 in 1 CARTON 1 1 mL in 1 VIAL, GLASS 2 NDC:60681-1905-2 50 in 1 CARTON 2 1 mL in 1 VIAL, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 01/19/1998 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)