Label: PLEO SAN BRUCEL- brucella melitensis liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-1235-1, 60681-1235-2 - 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 May 23, 2012
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
1235-2
Pleo® San BRUCEL
PORTABLE SIPS 6XOral Homeopathic Medicine
The original
SANUM®
brand remediesINDICATIONS: For temporary relief of
muscle aches.DIRECTIONS FOR USE: Snap off top
portion of sipping container. Insert glass
sipping straw.DOSAGE: 1–3 x weekly 1 sip.
INGREDIENTS: 1 mL contains Brucella
melitensis 6X, in a base of purified saline
solution.Tamper Evident: Do not use this product
if the glass vial is broken.convenient, disposable
single dose containers50 doses, each 1 mL
(.03 fl oz)Rev. 01/2012
704IN6XSE50US201
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INGREDIENTS AND APPEARANCE
PLEO SAN BRUCEL
brucella melitensis liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-1235 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength brucella melitensis (UNII: OQF85710LZ) (brucella melitensis - UNII:OQF85710LZ) brucella melitensis 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:60681-1235-1 10 in 1 CARTON 1 1 mL in 1 VIAL, GLASS 2 NDC:60681-1235-2 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)