ENURESIS HP
- Manufacturer
- Natural Creations, Inc. | OHM Pharma, Inc.
- Effective date
- 2012-11-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:04:06
Label at a glance#
ProductENURESIS HP
Active ingredientAPIS MELLIFERA, SILVER NITRATE, BARIUM CARBONATE, ATROPA BELLADONNA, CAUSTICUM, EQUISETUM HYEMALE, IODINE, WOOD CREOSOTE, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORUS, PULSATILLA VULGARIS, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS (HPUS*): Apis Mellifica 30C, Argentum Nitricum 30C, Baryta Carbonica 30C, Belladonna 30C, Causticum 30C, Equisetum Hyemale 30C, Iodium Purum 30C, Kreosotum 30C, Natrum Muriaticum 30C, Nitricum Acidum 30C, Phosphorus 30C, Pulsatilla 30C, Thuja Occidentalis 30C
INDICATIONS & USAGE SECTION
USES: Temporarily relieves involuntary urination, urging to urinate, bedwetting, incontinence, &/or other symptoms related to enuresis.
WARNINGS SECTION
WARNING:
Consult a physician for use inc hildren under 12 years of age. IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS: Adults and children above 12 yeears: 10 drops orally 3 times daily, or as directed by a health care professional.
OTC - DO NOT USE SECTION
OTHER INFORMATION: Tamper Seal: "Sealed for your protection."
Do not use if seal is broken or missing.
REFERENCES SECTION
n the product are officially monographed in the Homeopathic Pharmacopeia of the United States.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Purified Water, USP Ethanol Alcohol 20%
OTC - QUESTIONS SECTION
QUESTIONS AND COMMENTS?
MFG FOR: Natural Creations / Woodbine, IA / 51579 712.647.1600
OTC - PURPOSE SECTION
USES: Temporarily relieves involuntary urination, urging to urinate, bedwetting, incontinence, &/or other symptoms related to enuresis.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC: 43406-0020-1
ENURESIS HP
Enuresis
HOMEOPATHIC
1 fl oz (30 mL) / 20% Alcohol
UPC: 877730001320
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43406-0020-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-ebb2-cd31-e053-dbdaa90ab51a | ENURESIS HP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43406-0020-1 | ENURESIS HP | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43406-0020 | ENURESIS HP (APIS MELLIFERA 30C, SILVER NITRATE 30C, BARIUM CARBONATE 30C, ATROPA BELLADONNA 30C, CAUSTICUM 30C, EQUISETUM HYEMALE 30C, IODINE 30C, WOOD CREOSOTE 30C, SODIUM CHLORIDE 30C, NITRIC ACID 30C, PHOSPHORUS 30C, PULSATILLA VULGARIS 30C, THUJA OCCIDENTALIS LEAFY TWIG 30C) LIQUID [NATURAL CREATIONS, INC.] | 1 | Legacy NDC, 1 package rows | 20121106_62221e26-bcf4-4259-a1a4-aeca77093462.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| APIS MELLIFERA | ACTIVE INGREDIENT | 7S82P3R43Z | 1 | |
| ATROPA BELLADONNA | ACTIVE INGREDIENT | WQZ3G9PF0H | 1 | |
| BARIUM CARBONATE | ACTIVE INGREDIENT | 6P669D8HQ8 | 1 | |
| CAUSTICUM | ACTIVE INGREDIENT | DD5FO1WKFU | 1 | |
| EQUISETUM HYEMALE | ACTIVE INGREDIENT | 59677RXH25 | 1 | |
| IODINE | ACTIVE INGREDIENT | 9679TC07X4 | 1 | |
| NITRIC ACID | ACTIVE INGREDIENT | 411VRN1TV4 | 1 | |
| PHOSPHORUS | ACTIVE INGREDIENT | 27YLU75U4W | 1 | |
| PULSATILLA VULGARIS | ACTIVE INGREDIENT | I76KB35JEV | 1 | |
| SILVER NITRATE | ACTIVE INGREDIENT | 95IT3W8JZE | 1 | |
| SODIUM CHLORIDE | ACTIVE INGREDIENT | 451W47IQ8X | 1 | |
| THUJA OCCIDENTALIS LEAFY TWIG | ACTIVE INGREDIENT | 1NT28V9397 | 1 | |
| WOOD CREOSOTE | ACTIVE INGREDIENT | 3JYG22FD73 | 1 | |
| APIS MELLIFERA | ACTIVE MOIETY | 7S82P3R43Z | 1 | |
| ATROPA BELLADONNA | ACTIVE MOIETY | WQZ3G9PF0H | 1 | |
| BARIUM CATION | ACTIVE MOIETY | V645272HLN | 1 | |
| CAUSTICUM | ACTIVE MOIETY | DD5FO1WKFU | 1 | |
| EQUISETUM HYEMALE | ACTIVE MOIETY | 59677RXH25 | 1 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | 1 | |
| NITRIC ACID | ACTIVE MOIETY | 411VRN1TV4 | 1 | |
| PHOSPHORUS | ACTIVE MOIETY | 27YLU75U4W | 1 | |
| PULSATILLA VULGARIS | ACTIVE MOIETY | I76KB35JEV | 1 | |
| SILVER CATION | ACTIVE MOIETY | 57N7B0K90A | 1 | |
| SODIUM CATION | ACTIVE MOIETY | LYR4M0NH37 | 1 | |
| THUJA OCCIDENTALIS LEAFY TWIG | ACTIVE MOIETY | 1NT28V9397 | 1 | |
| WOOD CREOSOTE | ACTIVE MOIETY | 3JYG22FD73 | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- ENURESIS HP
- Apis Mellifera 30C, Silver Nitrate 30C, Barium Carbonate 30C, Atropa Belladonna 30C, Causticum 30C, Equisetum Hyemale 30C, Iodine 30C, Wood Creosote 30C, Sodium Chloride 30C, Nitric Acid 30C, Phosphorus 30C, Pulsatilla Vulgaris 30C, Thuja Occidentalis Leafy Twig 30C
- APIS MELLIFERA
- SILVER NITRATE
- SILVER CATION
- BARIUM CARBONATE
- BARIUM CATION
- ATROPA BELLADONNA
- CAUSTICUM
- EQUISETUM HYEMALE
- IODINE
- WOOD CREOSOTE
- SODIUM CHLORIDE
- SODIUM CATION
- NITRIC ACID
- PHOSPHORUS
- PULSATILLA VULGARIS
- THUJA OCCIDENTALIS LEAFY TWIG
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43406-0020 | 43406-0020-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| APIS MELLIFERA | 7S82P3R43Z | ACTIM |
| SILVER NITRATE | 95IT3W8JZE | ACTIM |
| BARIUM CARBONATE | 6P669D8HQ8 | ACTIM |
| ATROPA BELLADONNA | WQZ3G9PF0H | ACTIM |
| CAUSTICUM | DD5FO1WKFU | ACTIM |
| EQUISETUM HYEMALE | 59677RXH25 | ACTIM |
| IODINE | 9679TC07X4 | ACTIM |
| WOOD CREOSOTE | 3JYG22FD73 | ACTIM |
| SODIUM CHLORIDE | 451W47IQ8X | ACTIM |
| NITRIC ACID | 411VRN1TV4 | ACTIM |
| PHOSPHORUS | 27YLU75U4W | ACTIM |
| PULSATILLA VULGARIS | I76KB35JEV | ACTIM |
| THUJA OCCIDENTALIS LEAFY TWIG | 1NT28V9397 | ACTIM |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 0159af68-7743-4adf-bbce-ec7ce5016c16 | 62221e26-bcf4-4259-a1a4-aeca77093462 | 2012-11-01 | Warnings | 0159af68-7743-4adf-bbce-ec7ce5016c16 62221e26-bcf4-4259-a1a4-aeca77093462 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.