Bryophyllum Argento culta 3X

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Bryophyllum Argento culta 3X
Generic name: BRYOPHYLLUM ARGENTO CULTA 3X
Manufacturer: Uriel Pharmacy, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 4d7a929d-cbc9-6706-e063-6294a90a5e06
SPL ID: 4d7a929d-cbca-6706-e063-6294a90a5e06
Version: 1
Effective date: 2026-03-20
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:55:58

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Bryophyllum Argento culta 3X	openfda.brand_name
generic name		BRYOPHYLLUM ARGENTO CULTA 3X	openfda.generic_name
manufacturer name		Uriel Pharmacy, Inc	openfda.manufacturer_name
ndc	package	48951-2163-3	openfda.package_ndc
ndc	product	48951-2163	openfda.product_ndc
ndc11	package	48951216303	derived:openfda.package_ndc
spl id		4d7a929d-cbca-6706-e063-6294a90a5e06	id
spl set id		4d7a929d-cbc9-6706-e063-6294a90a5e06	set_id
unii		3M4G523W1G	openfda.unii
unii		L6X13JKL8O	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

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