Cuprum 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: Cuprum Metallicum
Generic name: CUPRUM METALLICUM
Manufacturer: OHM PHARMA INC.
Product type: HUMAN OTC DRUG
SPL set ID: c995ecc3-41f6-4f49-a8c2-fa282bdf6d26
SPL ID: d45eadc3-f555-3693-e053-2a95a90aab34
Version: 3
Effective date: 2021-12-30
Source export date: 2026-10-12
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:04:56

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		Cuprum Metallicum	openfda.brand_name
generic name		CUPRUM METALLICUM	openfda.generic_name
manufacturer name		OHM PHARMA INC.	openfda.manufacturer_name
ndc	package	66096-826-01	openfda.package_ndc
ndc	product	66096-826	openfda.product_ndc
ndc11	package	66096082601	derived:openfda.package_ndc
spl id		d45eadc3-f555-3693-e053-2a95a90aab34	id
spl set id		c995ecc3-41f6-4f49-a8c2-fa282bdf6d26	set_id
unii		789U1901C5	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: Keep out of reach of children. If pregnant or breast-feeding, ask a health care professional before use. Stop use and ask a health care professional if symptoms persist for more than 3 days or worsen. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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