Urtica Conchae

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2024-12-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:29:25

Label at a glance#

ProductUrtica Conchae

Active ingredientURTICA URENS, OSTREA EDULIS SHELL, TIN

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: Urtica urens (Small nettle) 3X, Conchae (Oyster shells) 6X, Stannum met. (Metallic tin) 12X

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. Do not use if allergic to any ingredient. Contains traces of lactose. 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

Urtica Conchae Ampules

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-9386-1	2026-01-29	C162847	48780-1	49896155-a5bb-586f-e063-e6dba90add90	Urtica Conchae

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-9386-1	Urtica Conchae	10 in 1 BOX	LIQUID	10		1
48951-9386-1	Urtica Conchae	1 mL in 1 AMPULE	LIQUID	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-9386	URTICA CONCHAE LIQUID [URIEL PHARMACY INC.]	1	2 package rows	20241210_28d842a5-58a8-0e52-e063-6294a90a1902.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Urtica Conchae
WATER
SODIUM CHLORIDE
LACTOSE
URTICA URENS
OSTREA EDULIS SHELL
TIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-9386	48951-9386-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
LACTOSE	J2B2A4N98G	IACT
URTICA URENS	IHN2NQ5OF9	ACTIB
OSTREA EDULIS SHELL	49OY13BE7Z	ACTIB
TIN	387GMG9FH5	ACTIB

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
28d83421-77c5-3c42-e063-6394a90ae773			28d842a5-58a8-0e52-e063-6294a90a1902	2024-12-09	Warnings	Exact identifier spl id: 28d83421-77c5-3c42-e063-6394a90ae773 spl set id: 28d842a5-58a8-0e52-e063-6294a90a1902

Reported adverse events (FAERS/openFDA)#

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