Cinis Equiseti 6X

Manufacturer: Uriel Pharmacy, Inc.
Effective date: 2024-11-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:29:02

Label at a glance#

ProductCinis Equiseti 6X

Active ingredientEQUISETUM ARVENSE TOP

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

DOSAGE & ADMINISTRATION SECTION

Take the contents of one ampule
under the tongue and hold for 30
seconds, then swallow.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Cinis Equiseti (Ash of horsetail herb) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt, Lactose

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

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains traces of lactose. 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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cinis Equiseti 6X Ampules

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-3273-3	Cinis Equiseti 6X	10 in 1 BOX	LIQUID	10		1
48951-3273-3	Cinis Equiseti 6X	2 mL in 1 AMPULE	LIQUID	2		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-3273	CINIS EQUISETI 6X LIQUID [URIEL PHARMACY, INC.]	1	2 package rows	20241123_277010ea-d864-d861-e063-6394a90abc5c.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Cinis Equiseti 6X
WATER
EQUISETUM ARVENSE TOP
SODIUM CHLORIDE
LACTOSE, UNSPECIFIED FORM
ANHYDROUS LACTOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-3273	48951-3273-3

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
EQUISETUM ARVENSE TOP	1DP6Y6B65Z	ACTIB
SODIUM CHLORIDE	451W47IQ8X	IACT
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	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
27700707-134c-b908-e063-6394a90a2367			277010ea-d864-d861-e063-6394a90abc5c	2024-11-21	Warnings	Exact identifier spl id: 27700707-134c-b908-e063-6394a90a2367 spl set id: 277010ea-d864-d861-e063-6394a90abc5c

Reported adverse events (FAERS/openFDA)#

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