Liverex I
Liverex I is an FDA drug label for the active ingredient GINKGO BILOBA, FEL TAURI, GALLBLADDER (SUIS), HEPAR SUIS), THYROIDINUM (SUIS), GERMANIUM SESQUIOXIDE, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALICUM ACIDUM, MANGANUM METALLICUM, PYRUVIC ACID, SUCCINICUM ACIDUM, NAPHTHOCHINONUM, ARSENICUM METALLICUM, SULPHUR, ACONITICUM ACIDUM, CIS, LYCOPODIUM CLAVATUM, NATRUM OXALACETICUM, PHOSPHORUS manufactured by Energique, Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230721.
Generic: GINKGO BILOBA, FEL TAURI, GALLBLADDER (SUIS), HEPAR SUIS), THYROIDINUM (SUIS), GERMANIUM SESQUIOXIDE, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALICUM ACIDUM, MANGANUM METALLICUM, PYRUVIC ACID, SUCCINICUM ACIDUM, NAPHTHOCHINONUM, ARSENICUM METALLICUM, SULPHUR, ACONITICUM ACIDUM, CIS, LYCOPODIUM CLAVATUM, NATRUM OXALACETICUM, PHOSPHORUS
Manufacturer: Energique, Inc.
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 44911-0419
Application:
Effective: 20230721
Active Ingredients: ACTIVE INGREDIENTS: (in each drop): 33.30% of Natrum Oxalaceticum 12X, 30X. 0.93% of Ginkgo Biloba 6X; Aconiticum Acidum, Cis 30X; Alpha-Ketoglutaricum Acidum 8X, 12X, 30X, Citricum Acidum 8X, 12X, 30X, Fumaricum Acidum 8X, 12X, 30X, Malicum Acidum 8X, 12X, 30X, Pyruvic Acid 8X, 12X, 30X; Arsenicum Metallicum 12X, Sulphur 12X; Fel Tauri 12X, 30X, Gallbladder (Suis) 12X, 30X, Hepar Suis 12X, 30X, Lycopodium Clavatum 12X, 30X, Manganum Metallicum 12X, 30X, Phosphorus 12X, 30X, Succinicum Acidum 12X, 30X, Thyroidinum (Suis) 12X, 30X; Naphthochinonum 30X. 0.01% of Fel Tauri 6X, Gallbladder (Suis) 6X, Hepar Suis 6X, Thyroidinum (Suis) 6X; Germanium Sesquioxide 8X, Manganum Metallicum 8X, Succinicum Acidum 8X; Naphthochinonum 9X, 12X; Aconiticum Acidum, Cis 12X.
Indications & Usage
INDICATIONS: May temporarily relieve abdominal pain and nausea.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dosage & Administration
DIRECTIONS: Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
Contraindications
Not available.
Warnings
WARNINGS: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
Adverse Reactions
Not available.
More from same ingredient
No related products.