Rose Copper

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: Rose Copper
Generic name: ROSE COPPER
Manufacturer: Uriel Pharmacy Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 6749923f-e896-496f-a8ff-7cf7a386b524
SPL ID: 2b247a51-97b4-e240-e063-6294a90a8907
Version: 7
Effective date: 2025-01-07
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:27:51

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		Rose Copper	openfda.brand_name
generic name		ROSE COPPER	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc.	openfda.manufacturer_name
ndc	package	48951-8348-5	openfda.package_ndc
ndc	product	48951-8348	openfda.product_ndc
ndc11	package	48951834805	derived:openfda.package_ndc
spl id		2b247a51-97b4-e240-e063-6294a90a8907	id
spl set id		6749923f-e896-496f-a8ff-7cf7a386b524	set_id
unii		T8BEA5064F	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.