DRUG FACTS:

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2026-04-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:38:18

Label at a glance#

ProductUrinary HP
Active ingredientBERBERIS VULGARIS ROOT BARK, LYTTA VESICATORIA, CAUSTICUM, CLEMATIS RECTA FLOWERING TOP, EQUISETUM HYEMALE WHOLE, CANIS LUPUS FAMILIARIS MILK, LYCOPODIUM CLAVATUM SPORE, MERCURY, PULSATILLA PRATENSIS WHOLE, SMILAX ORNATA WHOLE, SEPIA OFFICINALIS JUICE, STAPHISAGRIA MACROSPERMA SEED
Label structure9 sections

Indications and uses

May temporarily relieve symptoms of burning and irritation of the pelvis after urination and the urgent desire to urinate.** **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): 8.33% of Berberis Vulgaris 30X, Cantharis 30X, Causticum 30X, Clematis Erecta 30X, Equisetum Hyemale 30X, Lac Caninum 30X, Lycopodium Clavatum 30X, Mercurius Vivus 30X, Pulsatilla 30X, Sarsaparilla 30X, Sepia 30X, Staphysagria 30X.

PURPOSE:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of burning and irritation of the pelvis after urination and the urgent desire to urinate.**

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

WARNINGS:

WARNINGS SECTION

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.

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 burning and irritation of the pelvis after urination and the urgent desire to urinate.**

**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

URINARY HP

1 fl. oz. (30 ml)

URINARY HPURINARY HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0907-1Urinary HP30 mL in 1 BOTTLE, DROPPERLIQUID301

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-090744911-0907-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Urinary HPBERBERIS VULGARIS, CANTHARIS, CAUSTICUM, CLEMATIS ERECTA, EQUISETUM HYEMALE, LAC CANINUM, LYCOPODIUM CLAVATUM, MERCURIUS VIVUS, PULSATILLA (PRATENSIS), SARSAPARILLA (SMILAX REGELII), SEPIA, STAPHYSAGRIAEnergique, Inc.e26bd66d-615a-47e5-a042-26bbafcd200e2026-04-02WarningsExact identifier
ndc (package): 44911-0907-1
ndc (product): 44911-0907
ndc11 (package): 44911090701
spl id: e2678b9d-074f-45a9-9998-de1d11904d18
spl set id: e26bd66d-615a-47e5-a042-26bbafcd200e

Reported adverse events (FAERS/openFDA)#

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