FDA.reportPublic FDA data

Scorodite Prunus

Product NDC
48951-8169
11-digit product format
489518169
Labeler code
48951
Product ID
48951-8169_6dfeb1ce-37cd-228f-e053-2a91aa0ac12a
Type
HUMAN OTC DRUG
Nonproprietary name
Scorodite Prunus
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
CAMPHOR (NATURAL); VERATRUM ALBUM ROOT; SLOE; FERROUS ARSENATE; BOS TAURUS PITUITARY GLAND; GOLD
Active strength
4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
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 productproduct48951-8169IInactivated by FDA2026-10-05
excluded packagepackage48951-816948951-8169-2IInactivated 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
48951-8169-2Scorodite Prunus1350 in 1 BOTTLE, GLASSPELLET13504

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BOS TAURUS PITUITARY GLANDACTIVE INGREDIENT7JM57I419KSCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q941SCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
FERROUS ARSENATEACTIVE INGREDIENT129CO35H12SCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
GOLDACTIVE INGREDIENT79Y1949PYOSCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
SLOEACTIVE INGREDIENT3MLB4858X7SCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
VERATRUM ALBUM ROOTACTIVE INGREDIENTQNS6W5US1ZSCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
BOS TAURUS PITUITARY GLANDACTIVE MOIETY7JM57I419KSCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q941SCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
FERROUS ARSENATEACTIVE MOIETY129CO35H12SCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
GOLDACTIVE MOIETY79Y1949PYOSCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
SLOEACTIVE MOIETY3MLB4858X7SCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
VERATRUM ALBUM ROOTACTIVE MOIETYQNS6W5US1ZSCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GSCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554SCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8169SCORODITE PRUNUS PELLET [URIEL PHARMACY INC.]4Legacy NDC, 1 package rows20240514_b292a136-23e6-4bdf-a916-3236d8956b1e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8169-2489518169021350 PELLET in 1 BOTTLE, GLASS (48951-8169-2) 1350 pellet2009-09-010000-00-00NoNoCurrent