Label: PLEO NIG EX- aspergillus niger immunoserum rabbit liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-2111-1, 60681-2111-2 - 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
2111-1
Pleo™ Nig 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™ Nig.INGREDIENTS: 1 mL contains Aspergil-
lus niger 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 NIG EX
aspergillus niger immunoserum rabbit liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-2111 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Aspergillus niger immunoserum rabbit (UNII: 34I0G8739W) (Aspergillus niger immunoserum rabbit - UNII:34I0G8739W) Aspergillus niger 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:60681-2111-1 10 in 1 CARTON 1 1 mL in 1 VIAL, GLASS 2 NDC:60681-2111-2 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 08/19/1998 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)