FDA.reportPublic FDA data

Argentum Malachite

Product NDC
48951-1309
11-digit product format
489511309
Labeler code
48951
Product ID
48951-1309_38934e4c-eb56-377d-e063-6394a90aca94
Type
HUMAN OTC DRUG
Nonproprietary name
Argentum Malachite
Dosage form
CREAM
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
AZADIRACHTA INDICA FLOWER; CUPRIC CATION; MERCURY; SILVER
Active strength
2; 3; 6; 3 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Argentum Malachite
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CUPRIC CATION2 [hp_X]/g
MERCURY3 [hp_X]/g
SILVER6 [hp_X]/g
AZADIRACHTA INDICA FLOWER3 [hp_X]/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8CBV67279LInternal UNII lookup
FXS1BY2PGLInternal UNII lookup
3M4G523W1GInternal UNII lookup
3TE8A92UPMInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7a2d8d3c-2c47-5de9-e053-2a91aa0a8f08Available on FDA.report

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1309ARGENTUM MALACHITE CREAM [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 1 package rows20240213_7a2d8d3c-2c47-5de9-e053-2a91aa0a8f08.zip

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 (product): 48951-1309

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1309-54895113090560 g in 1 TUBE (48951-1309-5) 60 g2009-09-010000-00-00NoNoCurrent