![OLIVENITE 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]](https://medic.hrt.org//dailymed/images/f2a5265c-e827-4131-86f2-3b9c241a246a/Olivenite6SpecialOrderAmpule.jpg)
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
-
WARNINGS
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before usefor serious conditions or if conditions worsen or
persist. If pregnant or nursing, consult
a doctor before use. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
OLIVENITE 6 SPECIAL ORDER
olivenite 6 special order liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-7084 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COPPER ARSENATE (UNII: EV78GZO3YS) (COPPER ARSENATE - UNII:EV78GZO3YS) COPPER ARSENATE 6 [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:48951-7084-1 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(48951-7084)
