NDC 43742-0357

BIO GALLIUM

Betula (pendula), Cortex, Caltha Palustris, Clematis Erecta, Galium Aparine, Hedera Helix, Juniperus Communis, Sedum Acre, Sempervivum Tectorum, Thuja Occidentalis, Urtica Urens, Echinacea (angustifolia), Nitricum Acidum, Cortisone Aceticum, Argentum Metallicum, Calcarea Fluorica, Phosphorus, Aurum Metallicum, Apis Mellifica, Ononis Spinosa, Gaertner Bacillus (bach)

BIO GALLIUM is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Betula Pendula Bark; Caltha Palustris; Clematis Recta Flowering Top; Galium Aparine; Hedera Helix Flowering Twig; Juniper Berry; Sedum Acre; Sempervivum Tectorum Leaf; Thuja Occidentalis Leafy Twig; Urtica Urens; Echinacea Angustifolia; Nitric Acid; Cortisone Acetate; Silver; Calcium Fluoride; Phosphorus; Gold; Apis Mellifera; Ononis Spinosa Whole; Salmonella Enterica Subsp. Enterica Serovar Enteritidis.

Product ID43742-0357_b9f37537-08b4-4f2a-b43a-d442d8830e72
NDC43742-0357
Product TypeHuman Otc Drug
Proprietary NameBIO GALLIUM
Generic NameBetula (pendula), Cortex, Caltha Palustris, Clematis Erecta, Galium Aparine, Hedera Helix, Juniperus Communis, Sedum Acre, Sempervivum Tectorum, Thuja Occidentalis, Urtica Urens, Echinacea (angustifolia), Nitricum Acidum, Cortisone Aceticum, Argentum Metallicum, Calcarea Fluorica, Phosphorus, Aurum Metallicum, Apis Mellifica, Ononis Spinosa, Gaertner Bacillus (bach)
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2014-10-10
Marketing End Date2022-06-24
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDeseret Biologicals, Inc.
Substance NameBETULA PENDULA BARK; CALTHA PALUSTRIS; CLEMATIS RECTA FLOWERING TOP; GALIUM APARINE; HEDERA HELIX FLOWERING TWIG; JUNIPER BERRY; SEDUM ACRE; SEMPERVIVUM TECTORUM LEAF; THUJA OCCIDENTALIS LEAFY TWIG; URTICA URENS; ECHINACEA ANGUSTIFOLIA; NITRIC ACID; CORTISONE ACETATE; SILVER; CALCIUM FLUORIDE; PHOSPHORUS; GOLD; APIS MELLIFERA; ONONIS SPINOSA WHOLE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS
Active Ingredient Strength4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL
NDC Exclude FlagN

Packaging

NDC 43742-0357-1

30 mL in 1 BOTTLE, DROPPER (43742-0357-1)
Marketing Start Date2014-10-10
Marketing End Date2022-06-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43742-0357-1 [43742035701]

BIO GALLIUM LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-10-10
Inactivation Date2020-01-31

Drug Details


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