Agaricus comp. Phosphorus

Manufacturer: Uriel Pharmacy, Inc.
Effective date: 2024-11-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:29:01

Label at a glance#

ProductAgaricus comp. Phosphorus

Active ingredientPHOSPHORUS, SILVER, AMANITA MUSCARIA FRUITING BODY, OYSTER SHELL CALCIUM CARBONATE, CRUDE, DRYOPTERIS FILIX-MAS ROOT

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

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 Ingredients: Filix mas e rad (Male fern) 4X, Argentum met (Silver) 6X, Phosphorus (Yellow phosphorus) 6X, Calcarea carbonicum (nat.calcium carbonate) 7X, Agaricus muscarius (Fly agaric mushroom) 8X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled 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

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

Agaricus comp. Phosphorus Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1377-3	Agaricus comp. Phosphorus	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1377	AGARICUS COMP. PHOSPHORUS LIQUID [URIEL PHARMACY, INC.]	1	1 package rows	20241123_275ee04a-7955-22cd-e063-6394a90aa702.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Agaricus comp. Phosphorus
PHOSPHORUS
ALCOHOL
SILVER
AMANITA MUSCARIA FRUITING BODY
WATER
OYSTER SHELL CALCIUM CARBONATE, CRUDE
DRYOPTERIS FILIX-MAS ROOT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-1377	48951-1377-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PHOSPHORUS	27YLU75U4W	ACTIB
ALCOHOL	3K9958V90M	IACT
SILVER	3M4G523W1G	ACTIB
AMANITA MUSCARIA FRUITING BODY	DIF093I037	ACTIB
WATER	059QF0KO0R	IACT
OYSTER SHELL CALCIUM CARBONATE, CRUDE	2E32821G6I	ACTIB
DRYOPTERIS FILIX-MAS ROOT	C0ZK0RRF5X	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
275ee04a-7956-22cd-e063-6394a90aa702			275ee04a-7955-22cd-e063-6394a90aa702	2024-11-20	Warnings	Exact identifier spl id: 275ee04a-7956-22cd-e063-6394a90aa702 spl set id: 275ee04a-7955-22cd-e063-6394a90aa702

Reported adverse events (FAERS/openFDA)#

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