Argentum Quartz

Product NDC
48951-1098
11-digit product format
489511098
Labeler code
48951
Product ID
48951-1098_59f60153-eb18-e143-e063-6394a90a559c
Type
HUMAN OTC DRUG
Nonproprietary name
Argentum Quartz
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
SILVER; SILICON DIOXIDE
Active strength
20; 30 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Argentum Quartz
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILVER20 [hp_X]/mL
SILICON DIOXIDE30 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3M4G523W1GInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
765c8c8f-0727-45da-a77e-c3907a3d0793Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1098-1Argentum Quartz1 mL in 1 AMPULELIQUID14
48951-1098-1Argentum Quartz10 in 1 BOXLIQUID104

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
COLLOIDAL SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU4ARGENTUM QUARTZ LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE INGREDIENT3M4G523W1GARGENTUM QUARTZ LIQUID [URIEL PHARMACY INC.]1
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU4ARGENTUM QUARTZ LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE MOIETY3M4G523W1GARGENTUM QUARTZ LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XARGENTUM QUARTZ LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RARGENTUM QUARTZ LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1098ARGENTUM QUARTZ LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20241208_765c8c8f-0727-45da-a77e-c3907a3d0793.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 QuartzARGENTUM QUARTZUriel Pharmacy Inc.765c8c8f-0727-45da-a77e-c3907a3d07932026-08-26WarningsExact identifier
ndc (product): 48951-1098

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1098-14895110980110 AMPULE in 1 BOX (48951-1098-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent