Label: OLIVENITE 6 SPECIAL ORDER liquid
- NDC Code(s): 48951-7084-1
- Packager: Uriel Pharmacy Inc.
- 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 August 3, 2017
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
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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.
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
OLIVENITE 6 SPECIAL ORDER
olivenite 6 special order liquid
Product 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)