FDA.reportPublic FDA data

Aurum Prunus

Product NDC
48951-1203
11-digit product format
489511203
Labeler code
48951
Product ID
48951-1203_6a10217e-c0c4-4f4c-e053-2991aa0a3fcd
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 productproduct48951-1203IInactivated by FDA2026-10-05
excluded packagepackage48951-120348951-1203-3IInactivated by FDA2026-10-05

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-1203-32026-01-29C16284748780-149896155-a94a-586f-e063-e6dba90add90Aurum Prunus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1203-3Aurum Prunus60 mL in 1 BOTTLE, DROPPERLIQUID603

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
ALCOHOLINACTIVE INGREDIENT3K9958V90MAURUM 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
48951-1203AURUM PRUNUS LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 1 package rows20180417_31918b12-fa91-48bc-a420-71c668042b3c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1203-34895112030360 mL in 1 BOTTLE, DROPPER (48951-1203-3) 60 ml2009-09-010000-00-00NoNoCurrent