BHI Uri-Control

Manufacturer: MediNatura Inc
Effective date: 2023-04-13
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:20:55

Label at a glance#

ProductBHI Uri-Control

Active ingredientAPIS MELLIFERA, SILVER NITRATE, ATROPA BELLADONNA, LYTTA VESICATORIA, CAUSTICUM, EQUISETUM HYEMALE, PETROSELINUM CRISPUM, PULSATILLA VULGARIS, SMILAX ORNATA ROOT, TURPENTINE OIL

Label structure8 sections

Dosage and administration

Adults: 1-2 tablets 3 times per day or as directed by a health practitioner. Not to exceed 6 tablets per 24 hours. Children under 18, as directed by a health professional. Allow to completely dissolve in the mouth

Label contents#

Full prescribing information#

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Indications:

INDICATIONS & USAGE SECTION

For the temporary relief of minor
urinary pain and urgency.

Warnings:

WARNINGS SECTION

If pregnant or breast-feeding, ask a
health professional before use. Keep out of reach
of children. If symptoms persist or worsen, a
healthcare provider should be consulted. Do not use
if known sensitivity to BHI Uri-Control or any of its
ingredients exists.

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults: 1-2 tablets 3 times per day or
as directed by a health practitioner. Not to exceed 6
tablets per 24 hours. Children under 18, as
directed by a health professional. Allow to
completely dissolve in the mouth

Active ingredients:

OTC - ACTIVE INGREDIENT SECTION

Each 300 mg tablet contains:
*Apis mellifica 6X 30mg, Argentum nitricum 6X
30mg, *Belladonna 4X 30mg, *Cantharis 6X 30mg,
Causticum 8X 30mg, *Equisetum hyemale 6X 30mg,
*Petroselinum sativum 8X 30mg, *Pulsatilla 6X
30mg, *Sarsaparilla 6X 30mg, Terebinthina 8X 30mg.
*Natural

Inactive ingredients:

INACTIVE INGREDIENT SECTION

*Dextrose, *Lactose,
Magnesium stearate, *Maltodextrin
*contains one or more of these ingredients

Purpose

OTC - PURPOSE SECTION

Urinary Pain Relief

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BHI Uri-Control.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6cca4355-1206-91f7-02de-17eef38a8622	Product name	1	20140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62795-9004-2	2025-01-30	C162847	48780-1	2cef2736-b274-d83d-e063-dadaa90ab31f	BHI Uri-Control

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62795-9004-2	BHI Uri-Control	1 in 1 CARTON	TABLET	1		2
62795-9004-2	BHI Uri-Control	100 in 1 BOTTLE	TABLET	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62795-9004	BHI URI-CONTROL (APIS MELLIFERA, SILVER NITRATE, ATROPA BELLADONNA, LYTTA VESICATORIA, CAUSTICUM, EQUISETUM HYEMALE, PETROSELINUM CRISPUM, PULSATILLA VULGARIS, SMILAX REGELII ROOT, AND TURPENTINE OIL) TABLET [MEDINATURA INC]	2	Legacy NDC, 2 package rows	20230420_4d2184f0-30f3-4d8c-b51e-1a879be25640.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
62795-9004-2	EA - Each	62795-9004	ae0b4f1a-ef7f-49bf-8f43-428bf522c415	1	2022-05-04

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

BHI Uri-Control
APIS MELLIFERA, SILVER NITRATE, ATROPA BELLADONNA, LYTTA VESICATORIA, CAUSTICUM, EQUISETUM HYEMALE, PETROSELINUM CRISPUM, PULSATILLA VULGARIS, SMILAX REGELII ROOT, and TURPENTINE OIL
APIS MELLIFERA
SILVER NITRATE
SILVER CATION
ATROPA BELLADONNA
LYTTA VESICATORIA
CAUSTICUM
EQUISETUM HYEMALE
PETROSELINUM CRISPUM
PULSATILLA VULGARIS
ANEMONE PULSATILLA
SMILAX ORNATA ROOT
SARSAPARILLA
TURPENTINE OIL
LACTOSE
MAGNESIUM STEARATE
MALTODEXTRIN
DEXTROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62795-9004	62795-9004-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
APIS MELLIFERA	7S82P3R43Z	ACTIB
SILVER NITRATE	95IT3W8JZE	ACTIB
ATROPA BELLADONNA	WQZ3G9PF0H	ACTIB
LYTTA VESICATORIA	3Q034RO3BT	ACTIB
CAUSTICUM	DD5FO1WKFU	ACTIB
EQUISETUM HYEMALE	59677RXH25	ACTIB
PETROSELINUM CRISPUM	1WZA4Y92EX	ACTIB
PULSATILLA VULGARIS	I76KB35JEV	ACTIB
SMILAX ORNATA ROOT	2H1576D5WG	ACTIB
TURPENTINE OIL	C5H0QJ6V7F	ACTIB
LACTOSE	J2B2A4N98G	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
MALTODEXTRIN	7CVR7L4A2D	IACT
DEXTROSE	IY9XDZ35W2	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a9bfb09f-0839-4421-ad84-dc6ccc211a12			4d2184f0-30f3-4d8c-b51e-1a879be25640	2023-04-13	Warnings	Exact identifier spl id: a9bfb09f-0839-4421-ad84-dc6ccc211a12 spl set id: 4d2184f0-30f3-4d8c-b51e-1a879be25640

Reported adverse events (FAERS/openFDA)#

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