Renapath

Manufacturer
Energetix Corporation
Effective date
2026-08-11
Label type
HUMAN OTC DRUG LABEL
Version
13
Source
daily-update
Hydrated at
2026-08-14 00:01:06

Label at a glance#

ProductRenapath
Active ingredientCHONDRODENDRON TOMENTOSUM ROOT, PETROSELINUM CRISPUM, SUS SCROFA PITUITARY GLAND, RUBIA TINCTORUM ROOT, SARSAPARILLA, SOLIDAGO VIRGAUREA FLOWERING TOP, THYROID, BOVINE, ARCTOSTAPHYLOS UVA-URSI LEAF, BENZOIC ACID, BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA ROOT, HERRING SPERM DNA, EUTROCHIUM PURPUREUM ROOT, SUS SCROFA ADRENAL GLAND, HYDRANGEA ARBORESCENS ROOT, BOS TAURUS HYPOTHALAMUS, MERCURIC CHLORIDE, SUS SCROFA PANCREAS
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients 59.1 mL contains 3.44% of: Benzoicum ac 10X, 12X; Berber vulg 4X; Bryonia 12X; DNA 12X, 6C;  Eupatorium purp 12X; Glandula suprarenalis suis 9X, 12X, 6C; Merc corros 12X; Pancreas 9X, 12X, 6C; Pareira 10X, Petroselinum 4X; Pituitarum posterium 12X 6C; Rubia 6X; Sarsaparilla 4X, 6X; Solidago 4X; Thyroidinum 9X, 12X, 6C; Uva-ursi 4X.

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

INDICATIONS & USAGE SECTION

Uses Temporary relief of copious or diminished urination, occasional swelling in extremities.

WARNINGS SECTION

Warnings

In case of overdose, get medical help or contact a Poison Control Center right away.
If pregnant or breast feeding,ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Take 30 drops orally twice daily or as directed by a healthcare professional.
  • Consult a physician for use in children under 12 years of age or if symptoms worsen or persist.

OTHER SAFETY INFORMATION

Other information

  • Store at room temperature out of direct sunlight.
  • Do not use if neck wrap is broken or missing.
  • Shake well before use.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Cane Alcohol, Vegetable Glycerin, Purified Water.

OTC - QUESTIONS SECTION

Distributed by
Energetix Corp.
Dahlonega, GA 30533

Questions? 800.990.7085
www.energetix.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

energetix
Renapath
Homeopathic Remedy
Copious or diminished urination, occasional
swelling in extremities.
2 fl oz (59.1 mL) / 15% Cane Alcohol

Renapath r11-25 04071Renapath r11-25 04071

OTC - PURPOSE SECTION

Purpose Temporary relief of copious or diminished urination, occasional swelling in extremities.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARCTOSTAPHYLOS UVA-URSI LEAFACTIVE INGREDIENT3M5V3D1X363
BENZOIC ACIDACTIVE INGREDIENT8SKN0B0MIM3
BERBERIS VULGARIS ROOT BARKACTIVE INGREDIENT1TH8Q20J0U3
BOS TAURUS HYPOTHALAMUSACTIVE INGREDIENTS6G2NLH4Y73
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B3
CHONDRODENDRON TOMENTOSUM ROOTACTIVE INGREDIENT395A3P448Z3
EUTROCHIUM PURPUREUM ROOTACTIVE INGREDIENT0VYG5PVN5Q3
HERRING SPERM DNAACTIVE INGREDIENT51FI676N6F3
HYDRANGEA ARBORESCENS ROOTACTIVE INGREDIENTSFK828Q2DE3
MERCURIC CHLORIDEACTIVE INGREDIENT53GH7MZT1R3
PETROSELINUM CRISPUMACTIVE INGREDIENT1WZA4Y92EX3
RUBIA TINCTORUM ROOTACTIVE INGREDIENT0SVP95L23G3
SARSAPARILLAACTIVE INGREDIENT2H1576D5WG3
SOLIDAGO VIRGAUREA FLOWERING TOPACTIVE INGREDIENT5405K23S503
SUS SCROFA ADRENAL GLANDACTIVE INGREDIENT398IYQ16YV3
SUS SCROFA PANCREASACTIVE INGREDIENT9Y3J3362RY3
SUS SCROFA PITUITARY GLANDACTIVE INGREDIENTE8S87O660T3
THYROID, BOVINEACTIVE INGREDIENTMN18OTN73W3
ARCTOSTAPHYLOS UVA-URSI LEAFACTIVE MOIETY3M5V3D1X363
BENZOIC ACIDACTIVE MOIETY8SKN0B0MIM3
BERBERIS VULGARIS ROOT BARKACTIVE MOIETY1TH8Q20J0U3
BOS TAURUS HYPOTHALAMUSACTIVE MOIETYS6G2NLH4Y73
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B3
CHONDRODENDRON TOMENTOSUM ROOTACTIVE MOIETY395A3P448Z3
EUPATORIUM PURPUREUM ROOTACTIVE MOIETY0VYG5PVN5Q3
HERRING SPERM DNAACTIVE MOIETY51FI676N6F3
HYDRANGEA ARBORESCENS ROOTACTIVE MOIETYSFK828Q2DE3
MERCURIC CATIONACTIVE MOIETYED30FJ8Y423
PETROSELINUM CRISPUMACTIVE MOIETY1WZA4Y92EX3
RUBIA TINCTORUM ROOTACTIVE MOIETY0SVP95L23G3
SARSAPARILLAACTIVE MOIETY2H1576D5WG3
SOLIDAGO VIRGAUREA FLOWERING TOPACTIVE MOIETY5405K23S503
SUS SCROFA ADRENAL GLANDACTIVE MOIETY398IYQ16YV3
SUS SCROFA PANCREASACTIVE MOIETY9Y3J3362RY3
SUS SCROFA PITUITARY GLANDACTIVE MOIETYE8S87O660T3
THYROID, BOVINEACTIVE MOIETYMN18OTN73W3
ALCOHOLINACTIVE INGREDIENT3K9958V90M3
GLYCERININACTIVE INGREDIENTPDC6A3C0OX3
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64578-010364578-0103-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
122025-07-11full-release2026-06-01 02:34:25

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
RenapathBENZOICUM ACIDUM, BERBERIS VULGARIS, BRYONIA, DNA, EUPATORIUM PURPUREUM, GLANDULA SUPRARENALIS SUIS, HYDRANGEA ARBORESCENS, HYPOTHALAMUS, MERCURIUS CORROSIVUS, PANCREAS SUIS, PAREIRA BRAVA, PETROSELINUM SATIVUM, PITUITARUM POSTERIUM, RUBIA TINCTORUM, SARSAPARILLA, SOLIDAGO VIRGAUREA, THYROIDINUM (BOVINE), UVA-URSIEnergetix Corporation1a37b994-9470-4266-a4e1-008538ea0edf2026-08-11WarningsExact identifier
ndc (package): 64578-0103-1
ndc (product): 64578-0103
ndc11 (package): 64578010301
spl id: 58ca2513-a466-52d6-e063-6394a90a634c
spl set id: 1a37b994-9470-4266-a4e1-008538ea0edf

Reported adverse events (FAERS/openFDA)#

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