Label: PLEO REB- sus scrofa small intestine mucosa lymph follicle liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-3006-1, 60681-3006-2 - 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 January 6, 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
- Tamper Evident
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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 - 2 mL Carton
3006-1
Pleo™ Reb
PORTABLE SIPS 5XOral Homeopathic Medicine
INDICATIONS: For temporary relief of
occasional nausea and vomiting.DIRECTIONS FOR USE: Snap off top
portion of sipping container. Insert glass
sipping straw.DOSAGE: 1–3 × weekly 1 sip.
INGREDIENTS: 2 mL contains Peyer's
Patches Extrakt 5X, in a base of purified
saline solution. Tamper Evident: Do not
use this product if the glass vial is broken
or if imprinted security strip on carton is
torn.convenient, disposable
single dose containers50 doses, each 2 mL
(.06 fl oz)Rev. 12/2008
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INGREDIENTS AND APPEARANCE
PLEO REB
sus scrofa small intestine mucosa lymph follicle liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-3006 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength sus scrofa small intestine mucosa lymph follicle (UNII: 308LM01C72) (sus scrofa small intestine mucosa lymph follicle - UNII:308LM01C72) sus scrofa small intestine mucosa lymph follicle 5 [hp_X] in 2 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:60681-3006-1 10 in 1 CARTON 1 2 mL in 1 VIAL, GLASS 2 NDC:60681-3006-2 50 in 1 CARTON 2 2 mL in 1 VIAL, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 03/19/1997 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)