Equisetum 1% Special Order

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2018-06-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:10:11

Label at a glance#

ProductEquisetum 1% Special Order

Active ingredientEQUISETUM ARVENSE TOP

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Equisetum (Common horsetail) 2X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Organic sucrose

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. 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
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Equisetum1SpecialOrderPellets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-4145-2	Equisetum 1% Special Order	1350 in 1 BOTTLE, GLASS	PELLET	1350		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-4145	EQUISETUM 1% SPECIAL ORDER PELLET [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20180604_6dd368fd-687d-ce38-e053-2a91aa0a301a.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Equisetum 1% Special Order
EQUISETUM ARVENSE TOP
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-4145	48951-4145-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
EQUISETUM ARVENSE TOP	1DP6Y6B65Z	ACTIB
SUCROSE	C151H8M554	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
6dd368fd-687e-ce38-e053-2a91aa0a301a			6dd368fd-687d-ce38-e053-2a91aa0a301a	2018-06-04	Warnings	Exact identifier spl id: 6dd368fd-687e-ce38-e053-2a91aa0a301a spl set id: 6dd368fd-687d-ce38-e053-2a91aa0a301a

Reported adverse events (FAERS/openFDA)#

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