FDA.reportPublic FDA data

Enuresis

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2023-08-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:22:08

Label at a glance#

ProductEnuresis HP
Active ingredientSILVER NITRATE, ATROPA BELLADONNA, CAUSTICUM, EQUISETUM HYEMALE WHOLE, FERROSOFERRIC PHOSPHATE, WOOD CREOSOTE, NITRIC ACID, PULSATILLA PRATENSIS WHOLE, THUJA OCCIDENTALIS LEAFY TWIG, THYROID
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 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): 10.0% of Argentum Nitricum 30X, Belladonna 30X, Causticum 30X, Equisetum Hyemale 30X, Ferrum Phosphoricum 30X, Kreosotum 30X, Nitricum Acidum 30X, Pulsatilla 30X, Thuja Occidentalis 30X, Thyroidinum 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms due to bedwetting and abnormal bladder activity.**

**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.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms due to bedwetting and abnormal bladder activity.**

**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

ENURESIS HP

1 fl. oz. (30 ml)

ENURESIS HPENURESIS HP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0153-12022-03-09C16284748780-1ba0f9c33-4cf4-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0153-12021-01-29C16284748780-1ba0f9c33-4cf4-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0153-1EnuresisHP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0153ENURESIS HP (ARGENTUM NITRICUM, BELLADONNA, CAUSTICUM, EQUISETUM HYEMALE, FERRUM PHOSPHORICUM, KREOSOTUM, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), THUJA OCCIDENTALIS, THYROIDINUM (SUIS)) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20230825_257e63e2-c0d6-4fc8-9a93-14d9eb50bc09.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H1
CAUSTICUMACTIVE INGREDIENTDD5FO1WKFU1
EQUISETUM HYEMALEACTIVE INGREDIENT59677RXH251
FERROSOFERRIC PHOSPHATEACTIVE INGREDIENT91GQH8I5F71
NITRIC ACIDACTIVE INGREDIENT411VRN1TV41
PULSATILLA PRATENSISACTIVE INGREDIENT8E272251DI1
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZE1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
THYROID, PORCINEACTIVE INGREDIENT6RV024OAUQ1
WOOD CREOSOTEACTIVE INGREDIENT3JYG22FD731
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H1
CAUSTICUMACTIVE MOIETYDD5FO1WKFU1
EQUISETUM HYEMALEACTIVE MOIETY59677RXH251
FERROSOFERRIC PHOSPHATEACTIVE MOIETY91GQH8I5F71
NITRIC ACIDACTIVE MOIETY411VRN1TV41
PULSATILLA PRATENSISACTIVE MOIETY8E272251DI1
SILVER CATIONACTIVE MOIETY57N7B0K90A1
SUS SCROFA THYROIDACTIVE MOIETY6RV024OAUQ1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE MOIETY1NT28V93971
WOOD CREOSOTEACTIVE MOIETY3JYG22FD731
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-015344911-0153-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILVER NITRATE95IT3W8JZEACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
CAUSTICUMDD5FO1WKFUACTIB
EQUISETUM HYEMALE WHOLE59677RXH25ACTIB
FERROSOFERRIC PHOSPHATE91GQH8I5F7ACTIB
WOOD CREOSOTE3JYG22FD73ACTIB
NITRIC ACID411VRN1TV4ACTIB
PULSATILLA PRATENSIS WHOLE8E272251DIACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
THYROID6RV024OAUQACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 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
Enuresis HPARGENTUM NITRICUM, BELLADONNA, CAUSTICUM, EQUISETUM HYEMALE, FERRUM PHOSPHORICUM, KREOSOTUM, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), THUJA OCCIDENTALIS, THYROIDINUM (SUIS)Energique, Inc.257e63e2-c0d6-4fc8-9a93-14d9eb50bc092023-08-24WarningsExact identifier
ndc (package): 44911-0153-1
ndc (product): 44911-0153
ndc11 (package): 44911015301
spl id: 6a6fc5ba-8360-48de-8908-fbf32e4b99a6
spl set id: 257e63e2-c0d6-4fc8-9a93-14d9eb50bc09

Reported adverse events (FAERS/openFDA)#

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