FDA.reportPublic FDA data

Kidnex IV

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2026-02-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:37:44

Label at a glance#

ProductKidnex IV
Active ingredientGINKGO, OXOGLURIC ACID, ANHYDROUS CITRIC ACID, FUMARIC ACID, MALIC ACID, PYRUVIC ACID, SUCCINIC ACID, SILVER, GOLD, COPPER, GERMANIUM SESQUIOXIDE, MERCURY, STRYCHNOS NUX-VOMICA SEED, PORK KIDNEY, SUS SCROFA LYMPH, 1,4-NAPHTHOQUINONE, SODIUM DIETHYL OXALACETATE, PHOSPHORUS, SUS SCROFA URINARY BLADDER, ACONITIC ACID, (Z)-
Label structure9 sections

Indications and uses

May temporarily relieve symptoms of frequent urination and fluid retention.** **Claims based on traditional homeopathic practice, not accepted medical evidence, Not FDA evaluated.

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 for more than 7 days, 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

(in each drop): 2.63% of Aconiticum Acidum, Cis- 30X, Alpha-Ketoglutaricum Acidum 8X, 12X, 30X, Argentum Metallicum 12X, Aurum Metallicum 12X, Citricum Acidum 8X, 12X, 30X, Cuprum Metallicum 12X, Fumaricum Acidum 8X, 12X, 30X, Germanium Sesquioxide 12X, Ginkgo Biloba 6X, Kidney 12X, 30X, Lymph Node 12X, 30X, Malicum Acidum 8X, 12X, 30X, Mercurius Vivus 12X, Naphthochinonum 12X, 30X, Natrum Oxalaceticum 12X, 30X, Nux Vomica 12X, Phosphorus 12X, 30X, Pyruvic Acid 8X, 12X, 30X, Succinicum Acidum 8X, 12X, 30X, Urinary Bladder 12X, 30X.

PURPOSE:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of frequent urination and fluid retention.**

**Claims based on traditional homeopathic practice, not accepted medical evidence, Not FDA evaluated.

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

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 for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

USES:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms of frequent urination and fluid retention.**

**Claims based on traditional homeopathic practice, not accepted medical evidence, Not FDA evaluated.

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130363113701425GTIN-13: 0363113701425
EAN-13: 0363113701425
GTIN-12: 363113701425
UPC-A: 363113701425
GTIN storage (14 digits): 00363113701425		ENRG0747 Kidnex IV 06-23-25.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0747-1Kidnex IV30 mL in 1 BOTTLE, DROPPERLIQUID301

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-074744911-0747-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
GINKGO19FUJ2C58TACTIB
OXOGLURIC ACID8ID597Z82XACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLACTIB
FUMARIC ACID88XHZ13131ACTIB
MALIC ACID817L1N4CKPACTIB
PYRUVIC ACID8558G7RUTRACTIB
SUCCINIC ACIDAB6MNQ6J6LACTIB
SILVER3M4G523W1GACTIB
GOLD79Y1949PYOACTIB
COPPER789U1901C5ACTIB
GERMANIUM SESQUIOXIDE96WE91N25TACTIB
MERCURYFXS1BY2PGLACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PORK KIDNEYX7BCI5P86HACTIB
SUS SCROFA LYMPH33A7VYU29LACTIB
1,4-NAPHTHOQUINONERBF5ZU7R7KACTIB
SODIUM DIETHYL OXALACETATE6CA025Y4FGACTIB
PHOSPHORUS27YLU75U4WACTIB
SUS SCROFA URINARY BLADDER3G7U72W8DAACTIB
ACONITIC ACID, (Z)-OF5471ZHRRACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
Kidnex IVGINKGO BILOBA, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALICUM ACIDUM, PYRUVIC ACID, SUCCINICUM ACIDUM, ARGENTUM METALLICUM, AURUM METALLICUM, CUPRUM METALLICUM, GERMANIUM SESQUIOXIDE, MERCURIUS VIVUS, NUX VOMICA, KIDNEY (SUIS), LYMPH NODE (SUIS), NAPHTHOCHINONUM, NATRUM OXALACETICUM, PHOSPHORUS, URINARY BLADDER (SUIS), ACONITICUM ACIDUM, CIS-Energique, Inc.23de6b8e-7622-4ba6-89f7-37bd151687e22026-02-26WarningsExact identifier
ndc (package): 44911-0747-1
ndc (product): 44911-0747
ndc11 (package): 44911074701
spl id: f9c3c3d4-63ce-4b8e-a2b8-8e6acd48b769
spl set id: 23de6b8e-7622-4ba6-89f7-37bd151687e2

Reported adverse events (FAERS/openFDA)#

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