Equisetum cum sulfure tosta 6

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2024-02-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:25:59

Label at a glance#

ProductEquisetum cum sulfure tosta 6

Active ingredientEQUISETUM ARVENSE TOP, SULFUR

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older:
1/8 teaspoon. Ages 2-11: 1/16 teaspoon.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Equisetum cum Sulfure tosta (Equisetum, Sulfur) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Lactose

"prepared using rhythmical processes"

OTC - PURPOSE SECTION

Use: Temporary relief of urinary irritation.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Equisetum cum Sulfure tosta 6X Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-4182-4	Equisetum cum sulfure tosta 6	50 g in 1 BOTTLE, GLASS	POWDER	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-4182	EQUISETUM CUM SULFURE TOSTA 6 POWDER [URIEL PHARMACY INC.]	1	1 package rows	20240206_10a63c2d-e30d-2f92-e063-6394a90aff24.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Equisetum cum sulfure tosta 6
LACTOSE
EQUISETUM ARVENSE TOP
SULFUR

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-4182	48951-4182-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LACTOSE	J2B2A4N98G	IACT
EQUISETUM ARVENSE TOP	1DP6Y6B65Z	ACTIB
SULFUR	70FD1KFU70	ACTIB

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
10a59c42-d16e-0753-e063-6294a90a1e5c			10a63c2d-e30d-2f92-e063-6394a90aff24	2024-02-05	Warnings	Exact identifier spl id: 10a59c42-d16e-0753-e063-6294a90a1e5c spl set id: 10a63c2d-e30d-2f92-e063-6394a90aff24

Reported adverse events (FAERS/openFDA)#

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