Label: PLEO QUENT- penicillium glabrum suppository
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-2904-1 - Packager: Sanum Kehlbeck GmbH & Co. KG
- Category: HUMAN OTC DRUG LABEL
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 October 13, 2009
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- SPL UNCLASSIFIED SECTION
- Indications
- ACTIVE INGREDIENT PER DOSE
- Inactive ingredients
- DOSAGE
- WARNING
- STORAGE AND HANDLING
- Tamper Evident
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 10 Suppositories Carton
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INGREDIENTS AND APPEARANCE
PLEO QUENT
penicillium glabrum suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-2904 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength penicillium glabrum (UNII: 2IN23YUE0I) (penicillium glabrum - UNII:2IN23YUE0I) penicillium glabrum 3 [HP_X] Inactive Ingredients Ingredient Name Strength lactose (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-2904-1 1 in 1 CARTON 1 10 in 1 DOSE PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 03/19/1996 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)