FDA.reportPublic FDA data

Aurum Prunus

Product NDC
48951-1202
11-digit product format
489511202
Labeler code
48951
Product ID
48951-1202_6c69360b-2c2e-25a3-e053-2991aa0a6429
Type
HUMAN OTC DRUG
Nonproprietary name
Aurum Prunus
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
SLOE; GOLD
Active strength
6 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-1202IInactivated by FDA2026-10-05
excluded packagepackage48951-120248951-1202-1IInactivated by FDA2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1202-1Aurum Prunus1 mL in 1 AMPULELIQUID14
48951-1202-1Aurum Prunus10 in 1 BOXLIQUID104

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GOLDACTIVE INGREDIENT79Y1949PYOAURUM PRUNUS LIQUID [URIEL PHARMACY INC.]1
SLOEACTIVE INGREDIENT3MLB4858X7AURUM PRUNUS LIQUID [URIEL PHARMACY INC.]1
GOLDACTIVE MOIETY79Y1949PYOAURUM PRUNUS LIQUID [URIEL PHARMACY INC.]1
SLOEACTIVE MOIETY3MLB4858X7AURUM PRUNUS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XAURUM PRUNUS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RAURUM PRUNUS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1202AURUM PRUNUS LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20240919_38c658d0-6722-4fa6-8207-3941c5ca2090.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1202-14895112020110 AMPULE in 1 BOX (48951-1202-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent