Ignatia Bryophyllum

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2018-04-26
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:09:24

Label at a glance#

ProductIgnatia Bryophyllum

Active ingredientSTRYCHNOS IGNATII SEED, LACHESIS MUTA VENOM, SILVER, KALANCHOE DAIGREMONTIANA LEAF

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

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: Bryophyllum (Life plant) 3X, Ignatia (St. Ignatius’ bean) 4X, Lachesis (Bushmaster venom) 12X, Argentum (Silver) 10/20/30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 20% Organic cane alcohol

OTC - PURPOSE SECTION

Use: Temporary relief of hot flashes.

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
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IgnatiaBryophyllumSOLiquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8306-3	Ignatia Bryophyllum	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8306	IGNATIA BRYOPHYLLUM LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20180426_39bd979f-919e-0554-e054-00144ff8d46c.zip

Products#

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

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

Ignatia Bryophyllum
WATER
ALCOHOL
STRYCHNOS IGNATII SEED
LACHESIS MUTA VENOM
SILVER
KALANCHOE DAIGREMONTIANA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-8306	48951-8306-3

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
ALCOHOL	3K9958V90M	IACT
STRYCHNOS IGNATII SEED	1NM3M2487K	ACTIB
LACHESIS MUTA VENOM	VSW71SS07I	ACTIB
SILVER	3M4G523W1G	ACTIB
KALANCHOE DAIGREMONTIANA LEAF	L6X13JKL8O	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
6ac52a4d-c11a-560e-e053-2a91aa0a12b7			39bd979f-919e-0554-e054-00144ff8d46c	2018-04-26	Warnings	Exact identifier spl id: 6ac52a4d-c11a-560e-e053-2a91aa0a12b7 spl set id: 39bd979f-919e-0554-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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