Renatone

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2026-02-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:37:46

Label at a glance#

ProductRenatone
Active ingredientBERBERIS VULGARIS ROOT BARK, SOLIDAGO VIRGAUREA FLOWERING TOP, LYTTA VESICATORIA, ARSENIC TRIOXIDE, PROTORTONIA CACTI, LYCOPODIUM CLAVATUM SPORE, PHOSPHORUS, PACKERA AUREA WHOLE, STAPHISAGRIA MACROSPERMA SEED
Label structure9 sections

Indications and uses

May temporarily relieve urine that is scanty, dark, and offensive, pain in the back, and sensation as if some urine remained after urinating.** **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): 14.26% of Arsenicum Album 12X, Cantharis 12X, Coccus Cacti 12X, Lycopodium Clavatum 12X, Phosphorus 12X, Senecio Aureus 12X, Staphysagria 12X; 0.10% of Berberis Vulgaris 3X, Solidago Virgaurea 3X.

PURPOSE:

OTC - PURPOSE SECTION

May temporarily relieve urine that is scanty, dark, and offensive, pain in the back, and sensation as if some urine remained after urinating.**

**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 urine that is scanty, dark, and offensive, pain in the back, and sensation as if some urine remained after urinating.**

**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

RENATONE

1 fl. oz. (30 ml)

RENATONERENATONE

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130363113700831GTIN-13: 0363113700831
EAN-13: 0363113700831
GTIN-12: 363113700831
UPC-A: 363113700831
GTIN storage (14 digits): 00363113700831
ENRG0651 Renatone 10-21-25.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0904-1Renatone30 mL in 1 BOTTLE, DROPPERLIQUID301

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-090444911-0904-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
RenatoneBERBERIS VULGARIS, SOLIDAGO VIRGAUREA, CANTHARIS, ARSENICUM ALBUM, COCCUS CACTI, LYCOPODIUM CLAVATUM, PHOSPHORUS, SENECIO AUREUS, STAPHYSAGRIAEnergique, Inc.c2fbeb1b-a19f-4c09-947e-adbdabe256bf2026-02-27WarningsExact identifier
ndc (package): 44911-0904-1
ndc (product): 44911-0904
ndc11 (package): 44911090401
spl id: 42a3edb1-e870-417e-91e3-8db482f79e53
spl set id: c2fbeb1b-a19f-4c09-947e-adbdabe256bf

Reported adverse events (FAERS/openFDA)#

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