Label: PLEO REC- bacillus firmus capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 60681-3102-2 - 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 8, 2009
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- SPL UNCLASSIFIED SECTION
- Indications
- INGREDIENTS
- OTHER COMPONENTS
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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 taking this product. Keep this and all medications out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. Protect from light and heat.
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INGREDIENTS AND APPEARANCE
PLEO REC
bacillus firmus capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-3102 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength bacillus firmus (UNII: D6U864H4DT) (bacillus firmus - UNII:D6U864H4DT) bacillus firmus 4 [hp_X] Inactive Ingredients Ingredient Name Strength lactose (UNII: J2B2A4N98G) hypromellose (UNII: 3NXW29V3WO) Product Characteristics Color YELLOW Score no score Shape CAPSULE Size 19mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-3102-2 1 in 1 CARTON 1 5 in 1 BLISTER 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)