Label: VISCUM VITALIZER liquid
- NDC Code(s): 48951-9375-3
- 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.
Drug Label Information
Updated January 24, 2024
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
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ACTIVE INGREDIENT
Active Ingredients: Viscum album (Pini) (pine tree mistletoe) 3X, Bryophyllum e fol. (life plant) 6X, Equisetum (common horsetail) 6X, Silicea (silicon dioxide) 6X, Formica ex animale (red wood ant) 6X, Hepar (bovine liver) 6X, Magnesium hydroxydatum (magnesium hydroxide) 6X, Oxalis e pl. tota (wood sorrel) 6X, Prunus spinosa e flor. et summ. (blackthorn) 6X, Myrrh (myrrha resin) 6X, Olibanum (frankincense resin) 7X, Cuprum met. (copper) 8X, Phosphorus (yellow phosphorus) 8X, Aurum met. (metallic gold) 10X, Viscum album (Crataegi) (hawthorn tree mistletoe) 12X, Phoradendron leucarpum (Quercus) (oak tree mistletoe) 20X, Plumbum met. (lead with honey) 20X, Apis ex animale (honeybee) 21X, Argentum met. (silver) 30X
- 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. Contains lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.
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INGREDIENTS AND APPEARANCE
VISCUM VITALIZER
viscum vitalizer liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-9375 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FRANKINCENSE (UNII: R9XLF1R1WM) (FRANKINCENSE - UNII:R9XLF1R1WM) FRANKINCENSE 7 [hp_X] in 1 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 8 [hp_X] in 1 mL HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (HAWTHORN LEAF WITH FLOWER - UNII:6OM09RPY36) HAWTHORN LEAF WITH FLOWER 12 [hp_X] in 1 mL VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP 3 [hp_X] in 1 mL APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 21 [hp_X] in 1 mL MYRRH (UNII: JC71GJ1F3L) (MYRRH - UNII:JC71GJ1F3L) MYRRH 7 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 8 [hp_X] in 1 mL LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD 20 [hp_X] in 1 mL BEEF LIVER (UNII: W8N8R55022) (BEEF LIVER - UNII:W8N8R55022) BEEF LIVER 6 [hp_X] in 1 mL SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 30 [hp_X] in 1 mL EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP 6 [hp_X] in 1 mL MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 6 [hp_X] in 1 mL PHORADENDRON LEUCARPUM FRUITING TOP (UNII: 3M834XM81W) (PHORADENDRON LEUCARPUM FRUITING TOP - UNII:3M834XM81W) PHORADENDRON LEUCARPUM FRUITING TOP 20 [hp_X] in 1 mL SLOE (UNII: 3MLB4858X7) (SLOE - UNII:3MLB4858X7) SLOE 6 [hp_X] in 1 mL GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 10 [hp_X] in 1 mL KALANCHOE DAIGREMONTIANA LEAF (UNII: L6X13JKL8O) (KALANCHOE DAIGREMONTIANA LEAF - UNII:L6X13JKL8O) KALANCHOE DAIGREMONTIANA LEAF 6 [hp_X] in 1 mL FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA 6 [hp_X] in 1 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6 [hp_X] in 1 mL OXALIS STRICTA WHOLE (UNII: 3STW243384) (OXALIS STRICTA WHOLE - UNII:3STW243384) OXALIS STRICTA WHOLE 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-9375-3 60 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 09/01/2009 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(48951-9375)