Label: PLEO MUC- mucor racemosus liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-1808-1, 60681-1808-2 - 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 November 11, 2009
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- SPL UNCLASSIFIED SECTION
- INDICATIONS
- DIRECTIONS FOR USE
- DOSAGE
- INGREDIENTS
- WARNING
- STORAGE AND HANDLING
- Tamper Evident
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 1 mL Carton
1808-2
Pleo™ Muc
PORTABLE SIPS 7XOral Homeopathic Medicine
INDICATIONS: For temporary relief of pain of
bruises, sprains, swelling of joints and muscles.DIRECTIONS FOR USE: Snap off top
portion of sipping container. Insert glass
sipping straw.DOSAGE: 1 SIP, twice weekly.
INGREDIENTS: 1 mL contains Mucor
racemosus 7X, in a base of purified sa-
line solution.convenient, disposable
single dose containers50 doses, each 1 mL
(.03 fl oz)Rev. 11/97
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INGREDIENTS AND APPEARANCE
PLEO MUC
mucor racemosus liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-1808 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength mucor racemosus (UNII: 17RH99LQ7G) (mucor racemosus - UNII:17RH99LQ7G) mucor racemosus 7 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) sodium chloride (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-1808-1 10 in 1 CARTON 1 1 mL in 1 VIAL, GLASS 2 NDC:60681-1808-2 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 01/01/1998 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)