FDA.reportPublic FDA data

EQUISETUM ARVENSE TOP

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-05
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:29:22

Label at a glance#

ProductSilica comp.
Active ingredientEQUISETUM ARVENSE TOP, QUERCUS ROBUR WHOLE, BEEF HEART, MAMMAL LIVER, SUS SCROFA PANCREAS, SUS SCROFA LUNG, PORK KIDNEY, BOS TAURUS CARTILAGE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take regularly before meals with a small amount of water. Ages 12 and older: 1 teaspoon. Ages 2-11: 1/2 teaspoon. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Cinis equiseti (Ash of horsetail herb) 5X, Cinis quercus (Oak bark ash) 9X, Cor (Bovine heart) 9X, Hepar (Bovine liver) 9X, Pancreas (Bovine pancreas) 9X, Pulmo (Bovine lung) 9X, Quercus e cort. (Oak bark) 9X, Renes (Porcine kidneys) 9X, Mesenchyme (Bovine embryonic connective tissue) 11X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Lactose, Bee pollen, Diatomaceous earth, Anise oil

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: To promote skin elasticity and strengthen hair and nails.

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
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Silica comp. PowderSilica comp. Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8327-4Silica comp.100 g in 1 BOTTLE, GLASSPOWDER1006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8327SILICA COMP. POWDER [URIEL PHARMACY INC.]6Legacy NDC, 1 package rows20241208_6bb681e9-0fce-7e5c-e053-2991aa0a7c65.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-832748951-8327-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
QUERCUS ROBUR WHOLER7QMG0BT2WACTIB
BEEF HEARTP47W069U38ACTIB
BEE POLLEN3729L8MA2CIACT
DIATOMACEOUS EARTH2RF6EJ0M85IACT
MAMMAL LIVERD0846624BIACTIB
SUS SCROFA PANCREAS9Y3J3362RYACTIB
SUS SCROFA LUNG7GL3G1COB3ACTIB
PORK KIDNEYX7BCI5P86HACTIB
BOS TAURUS CARTILAGEUE77B10IIYACTIB
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
ANISE OIL6Y89129C8HIACT

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
2888e910-b3b4-d430-e063-6394a90a8f326bb681e9-0fce-7e5c-e053-2991aa0a7c652024-12-05WarningsExact identifier
spl id: 2888e910-b3b4-d430-e063-6394a90a8f32
spl set id: 6bb681e9-0fce-7e5c-e053-2991aa0a7c65

Reported adverse events (FAERS/openFDA)#

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