FDA.reportPublic FDA data

Equisetum Silicea

Manufacturer
Uriel Pharmacy Inc.
Effective date
2026-03-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:38:13

Label at a glance#

ProductEquisetum Silicea
Active ingredientEQUISETUM ARVENSE TOP, SILICON DIOXIDE
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 Silicea culta (Common horsetail, Colloidal silicon dioxide) 3X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, 20% Organic cane alcohol

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

KEEP OUT OF REACH OF CHILDREN.
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 shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Equisetum Silicea LiquidEquisetum Silicea Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4039-3Equisetum Silicea60 mL in 1 BOTTLE, DROPPERLIQUID605

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
COLLOIDAL SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65Z1
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65Z1
PROPOLIS WAXINACTIVE INGREDIENT6Y8XYV2NOF1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-403948951-4039-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
WATER059QF0KO0RIACT
SILICON DIOXIDEETJ7Z6XBU4ACTIB
ALCOHOL3K9958V90MIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Equisetum SiliceaEQUISETUM SILICEAUriel Pharmacy Inc.e88b820b-4a07-42e2-8fe2-b30729e91a8c2026-03-30WarningsExact identifier
ndc (package): 48951-4039-3
ndc (product): 48951-4039
ndc11 (package): 48951403903
spl id: 4e43eb39-76aa-f806-e063-6394a90af572
spl set id: e88b820b-4a07-42e2-8fe2-b30729e91a8c

Reported adverse events (FAERS/openFDA)#

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