Kidnex

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2021-08-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:37:20

Label at a glance#

ProductKidnex IV
Active ingredientGINKGO, PORK KIDNEY, SUS SCROFA LYMPH, SUS SCROFA URINARY BLADDER, GERMANIUM SESQUIOXIDE, SILVER, GOLD, COPPER, MERCURY, OXOGLURIC ACID, ANHYDROUS CITRIC ACID, FUMARIC ACID, MALIC ACID, PYRUVIC ACID, SUCCINIC ACID, 1,2-NAPHTHOQUINONE, STRYCHNOS NUX-VOMICA SEED, ACONITIC ACID, (Z)-, SODIUM DIETHYL OXALACETATE, PHOSPHORUS
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Ginkgo Biloba 6X, Kidney (Suis) 6X, 12X, 30X, Lymph Node (Suis) 6X, 12X, 30X, Urinary Bladder (Suis) 6X, 12X, 30X, Germanium Sesquioxide 8X, Argentum Metallicum 8X, 12X, Aurum Metallicum 8X, 12X, Cuprum Metallicum 8X, 12X, Mercurius Vivus 8X, 12X, 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, Succinicum Acidum 8X, 12X, 30X, Naphthochinonum 9X, 12X, 30X, Nux Vomica 12X, Aconiticum Acidum, Cis- 12X, 30X, Natrum Oxalaceticum 12X, 30X, Phosphorus 12X, 30X.

INDICATIONS:

OTC - PURPOSE SECTION

Kidney, Bladder support.**


**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, 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.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

Kidney, Bladder support.**


**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579   800-869-8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

KIDNEX IV

1 fl. oz. (30 ml)

Kidnex IVKidnex IV

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-044144911-0441-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
418f132e-da8b-4dbe-8595-2f12575d6a4f79211bca-f727-4bd1-b8fb-97e5cf0995c82021-08-25WarningsExact identifier
spl id: 418f132e-da8b-4dbe-8595-2f12575d6a4f
spl set id: 79211bca-f727-4bd1-b8fb-97e5cf0995c8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.