- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. Contains traces of
lactose. If pregnant or nursing, consult a doctor before use. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PYRITE SALVIA
pyrite salvia liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8103 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE 3 [hp_X] in 1 mL ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN) (ANGELICA ARCHANGELICA ROOT - UNII:DTN01M69SN) ANGELICA ARCHANGELICA ROOT 5 [hp_X] in 1 mL HYOSCYAMUS NIGER LEAF (UNII: 32IT7G8BAW) (HYOSCYAMUS NIGER LEAF - UNII:32IT7G8BAW) HYOSCYAMUS NIGER LEAF 7 [hp_X] in 1 mL FERROUS DISULFIDE (UNII: 132N09W4PR) (FERROUS CATION - UNII:GW89581OWR) FERROUS DISULFIDE 7 [hp_X] in 1 mL SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 15 [hp_X] in 1 mL HYACINTHUS ORIENTALIS WHOLE (UNII: 33J37WGZ7H) (HYACINTHUS ORIENTALIS WHOLE - UNII:33J37WGZ7H) HYACINTHUS ORIENTALIS WHOLE 17 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) LACTOSE (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-8103-1 10 in 1 BOX 09/01/2009 1 1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009 Labeler - Uriel Pharmacy Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc. 043471163 manufacture(48951-8103)