Label: PLEO SANUVIS- lactic acid, l- ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-6301-1 - 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 June 4, 2010
If you are a consumer or patient please visit this version.
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- SPL UNCLASSIFIED SECTION
- Indications
- 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.
- INGREDIENTS
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30g Tube Carton
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INGREDIENTS AND APPEARANCE
PLEO SANUVIS
lactic acid, l- ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-6301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength lactic acid, l- (UNII: F9S9FFU82N) (lactic acid, l- - UNII:F9S9FFU82N) lactic acid, l- 1 [hp_X] in 30 g Inactive Ingredients Ingredient Name Strength glyceryl monostearate (UNII: 230OU9XXE4) lanolin alcohols (UNII: 884C3FA9HE) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-6301-1 1 in 1 CARTON 1 30 g in 1 TUBE 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)