FDA.reportPublic FDA data

Argentum Malachite

Manufacturer
Uriel Pharmacy Inc.
Effective date
2025-06-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:34:09

Label at a glance#

ProductArgentum Malachite
Active ingredientCUPRIC CATION, MERCURY, SILVER, AZADIRACHTA INDICA FLOWER
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: Neem extract 2X, Argentum met. (Silver) 3X, Malachite (Copper carbonate) 3X, Mercurius vivus (Mercury) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Spring water, Organic vinegar, Stearic acid, Glycerin, Isopropyl myristate, Lavender oil, Mineral oil, Povidone-iodine, Rosemary oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Sorbic acid, Tea tree oil, Frankincense oil, Myrrh oil, Grapefruit seed extract

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of athlete's foot.

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
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Argentum Malachite CreamArgentum Malachite Cream

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1309-5Argentum Malachite60 g in 1 TUBECREAM604

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-130948951-1309-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAVENDER OILZBP1YXW0H8IACT
MINERAL OILT5L8T28FGPIACT
CUPRIC CATION8CBV67279LACTIM
MERCURYFXS1BY2PGLACTIB
WATER059QF0KO0RIACT
STEARIC ACID4ELV7Z65APIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
POVIDONE-IODINE85H0HZU99MIACT
SILVER3M4G523W1GACTIB
ROSEMARY OIL8LGU7VM393IACT
CETYL ALCOHOL936JST6JCNIACT
STEARYL ALCOHOL2KR89I4H1YIACT
SORBIC ACIDX045WJ989BIACT
TEA TREE OILVIF565UC2GIACT
POLYOXYL 40 STEARATE13A4J4NH9IIACT
XANTHAN GUMTTV12P4NEEIACT
FRANKINCENSE OIL67ZYA5T02KIACT
MYRRH OILH74221J5J4IACT
CITRUS PARADISI SEED12F08874Y7IACT
AZADIRACHTA INDICA FLOWER3TE8A92UPMACTIB
ACETIC ACIDQ40Q9N063PIACT
GLYCERINPDC6A3C0OXIACT

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
Argentum MalachiteARGENTUM MALACHITEUriel Pharmacy Inc.7a2d8d3c-2c47-5de9-e053-2a91aa0a8f082025-06-27WarningsExact identifier
ndc (package): 48951-1309-5
ndc (product): 48951-1309
ndc11 (package): 48951130905
spl id: 38934e4c-eb56-377d-e063-6394a90aca94
spl set id: 7a2d8d3c-2c47-5de9-e053-2a91aa0a8f08

Reported adverse events (FAERS/openFDA)#

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