Cuprum 5

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 5
Generic name: CUPRUM 5
Manufacturer: Uriel Pharmacy Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 6c6ffab3-985a-49f2-9de5-a0736d5d85cf
SPL ID: 38933081-777e-57d2-e063-6294a90aba69
Version: 6
Effective date: 2025-06-27
Source export date: 2026-11-06
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:44:35

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		Cuprum 5	openfda.brand_name
generic name		CUPRUM 5	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc.	openfda.manufacturer_name
ndc	package	48951-3138-5	openfda.package_ndc
ndc	product	48951-3138	openfda.product_ndc
ndc11	package	48951313805	derived:openfda.package_ndc
spl id		38933081-777e-57d2-e063-6294a90aba69	id
spl set id		6c6ffab3-985a-49f2-9de5-a0736d5d85cf	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: 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, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. 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.