Millefolium 2X

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: Millefolium 2X
Generic name: MILLEFOLIUM 2X
Manufacturer: Uriel Pharmacy, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 36eaca5c-9015-cfb4-e063-6294a90a325c
SPL ID: 36eaca5c-9016-cfb4-e063-6294a90a325c
Version: 1
Effective date: 2025-06-06
Source export date: 2026-10-27
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:51:32

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Millefolium 2X	openfda.brand_name
generic name		MILLEFOLIUM 2X	openfda.generic_name
manufacturer name		Uriel Pharmacy, Inc	openfda.manufacturer_name
ndc	package	48951-7218-3	openfda.package_ndc
ndc	product	48951-7218	openfda.product_ndc
ndc11	package	48951721803	derived:openfda.package_ndc
spl id		36eaca5c-9016-cfb4-e063-6294a90a325c	id
spl set id		36eaca5c-9015-cfb4-e063-6294a90a325c	set_id
unii		2FXJ6SW4PK	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.