Label: BERBERIS VISCUM liquid
- NDC Code(s): 48951-2058-1
- 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.
Drug Label Information
Updated January 7, 2025
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
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ACTIVE INGREDIENT
Active Ingredients: Berberis (Barberry) 2X, Oxalis (Wood sorrel) 3X, Urtica urens (Small nettle) 3X, Viscum Mali (Apple tree mistletoe) 4X, Magnesium sulf. (Magnesium sulfate) 6X, Ovaria (Bovine ovaries) 6X, Sardonyx (Semiprecious stone) 6X, Uterus (Bovine uterus) 6X, Granite (Primitive rock containing quartz, feldspar, mica) 10X
- 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
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INGREDIENTS AND APPEARANCE
BERBERIS VISCUM
berberis viscum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-2058 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 2 [hp_X] in 1 mL OXALIS ACETOSELLA LEAF (UNII: U1W3U02EW0) (OXALIS ACETOSELLA LEAF - UNII:U1W3U02EW0) OXALIS ACETOSELLA LEAF 3 [hp_X] in 1 mL URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS 3 [hp_X] in 1 mL VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP 4 [hp_X] in 1 mL MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE, UNSPECIFIED 6 [hp_X] in 1 mL BOS TAURUS OVARY (UNII: 66LZN1C747) (BOS TAURUS OVARY - UNII:66LZN1C747) BOS TAURUS OVARY 6 [hp_X] in 1 mL ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE 6 [hp_X] in 1 mL BOS TAURUS UTERUS (UNII: 9169LW451G) (BOS TAURUS UTERUS - UNII:9169LW451G) BOS TAURUS UTERUS 6 [hp_X] in 1 mL PENOXSULAM (UNII: 784ELC1SCZ) (PENOXSULAM - UNII:784ELC1SCZ) PENOXSULAM 10 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-2058-1 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(48951-2058)
