Equisetum ex herba 1% Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:36

Label at a glance#

ProductEquisetum ex herba 1% Special Order
Active ingredientEQUISETUM ARVENSE TOP
Label structure9 sections

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: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Equisetum (Common horsetail) 2X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Organic cane alcohol

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. 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
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EquisetumExHerba1SOLiquidEquisetumExHerba1SOLiquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4138-3Equisetum ex herba 1% Special Order60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4138EQUISETUM EX HERBA 1% SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20180505_6b670483-0b3a-6a0b-e053-2991aa0a4066.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-413848951-4138-3

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
NameUNIIKind
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML · Source PDF

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
6b670483-0b3b-6a0b-e053-2991aa0a40666b670483-0b3a-6a0b-e053-2991aa0a40662018-05-04WarningsExact identifier
spl id: 6b670483-0b3b-6a0b-e053-2991aa0a4066
spl set id: 6b670483-0b3a-6a0b-e053-2991aa0a4066

Reported adverse events (FAERS/openFDA)#

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