Label: PLEO SANUVIS- lactic acid, l- tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-6303-1 - 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 30, 2013
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- PURPOSE
- Indications
- INGREDIENTS
- Tamper Evident
- DOSAGE
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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
- PRINCIPAL DISPLAY PANEL - 80 Tablet Carton
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INGREDIENTS AND APPEARANCE
PLEO SANUVIS
lactic acid, l- tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-6303 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength lactic acid, l- (UNII: F9S9FFU82N) (lactic acid, l- - UNII:F9S9FFU82N) lactic acid, l- 200 [hp_X] Inactive Ingredients Ingredient Name Strength Lactose (UNII: J2B2A4N98G) Starch, Potato (UNII: 8I089SAH3T) Magnesium Stearate (UNII: 70097M6I30) Product Characteristics Color WHITE Score no score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-6303-1 1 in 1 CARTON 1 80 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 06/15/2010 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)