Ferrum Metallicum

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: Ferrum Metallicum
Generic name: FERRUM METALLICUM
Manufacturer: True Botanica, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 88edb60a-96f9-4b90-854e-073f8f33ef97
SPL ID: 2bafb2f6-d7e5-77da-e063-6294a90a2a64
Version: 3
Effective date: 2025-01-14
Source export date: 2026-11-06
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:04:31

Harmonized routes table
Harmonized routes
TOPICAL

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		Ferrum Metallicum	openfda.brand_name
generic name		FERRUM METALLICUM	openfda.generic_name
manufacturer name		True Botanica, LLC	openfda.manufacturer_name
ndc	package	53645-1080-1	openfda.package_ndc
ndc	product	53645-1080	openfda.product_ndc
ndc11	package	53645108001	derived:openfda.package_ndc
spl id		2bafb2f6-d7e5-77da-e063-6294a90a2a64	id
spl set id		88edb60a-96f9-4b90-854e-073f8f33ef97	set_id
unii		E1UOL152H7	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: For external use only. Do not apply on open wounds, damaged skin or eyes. Consult your health care provider if symptoms persist more than 5 days or worsen or rash occurs. Do not use if allergic to any of the ingredients.

Reported adverse events (FAERS/openFDA)#

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