Label: PLEO SAN STAPH- staphylococcus aureus solution/ drops
- 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.
Updated November 11, 2011
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- Tamper Evident
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.
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.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton
INGREDIENTS AND APPEARANCE
PLEO SAN STAPH
staphylococcus aureus solution/ drops
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-1284 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength staphylococcus aureus (UNII: O478WX4004) (staphylococcus aureus - UNII:O478WX4004) staphylococcus aureus 6 [hp_X] in 10 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-1284-1 1 in 1 CARTON 1 10 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 09/19/1997 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)