Label: PLEO REB- sus scrofa small intestine mucosa lymph follicle suppository
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-3003-1 - 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 January 6, 2010
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- Official Label (Printer Friendly)
- 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 REB
sus scrofa small intestine mucosa lymph follicle suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-3003 Route of Administration RECTAL 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 4 [hp_X] Inactive Ingredients Ingredient Name Strength lactose (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-3003-1 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)