Cuprum 0.4

Manufacturer
Uriel Pharmacy, Inc | Uriel, Pharmacy, Inc
Effective date
2025-01-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:31:32

Label at a glance#

ProductCuprum 0.4
Active ingredientCOPPER
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100 gm contains: 4 gm Cuprum (Copper) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Yellow Petrolatum, White mineral Oil

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: Temporary relief of cold hands and feet.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

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.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cuprum 0.4 OintmentCuprum 0.4 Ointment

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3280-2Cuprum 0.430 g in 1 TUBEOINTMENT301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3280CUPRUM 0.4 OINTMENT [URIEL PHARMACY, INC]1Current NDC, 1 package rows20250127_2c8fc7ec-a8fe-7468-e063-6294a90ae355.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-328048951-3280-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
COPPER789U1901C5ACTIB
PETROLATUM4T6H12BN9UIACT
MINERAL OILT5L8T28FGPIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cuprum 0.4CUPRUM 0.4Uriel Pharmacy, Inc2c8fc7ec-a8fe-7468-e063-6294a90ae3552025-01-25WarningsExact identifier
ndc (package): 48951-3280-2
ndc (product): 48951-3280
ndc11 (package): 48951328002
spl id: 2c8fc7ec-a8ff-7468-e063-6294a90ae355
spl set id: 2c8fc7ec-a8fe-7468-e063-6294a90ae355

Reported adverse events (FAERS/openFDA)#

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