Home NDC 48951-8168 Scorodite Prunus
Product NDC 48951-8168
11-digit product format 489518168
Labeler code 48951
Product ID 48951-8168_2c28a030-bb5c-fb37-e063-6294a90aa38f
Type HUMAN OTC DRUG
Nonproprietary name Scorodite Prunus
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance CAMPHOR (NATURAL); VERATRUM ALBUM ROOT; SLOE; FERROUS ARSENATE; BOS TAURUS PITUITARY GLAND; GOLD
Active strength 4; 4; 6; 6; 8; 10 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 Scorodite Prunus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (NATURAL) 4 [hp_X]/mL VERATRUM ALBUM ROOT 4 [hp_X]/mL SLOE 6 [hp_X]/mL FERROUS ARSENATE 6 [hp_X]/mL BOS TAURUS PITUITARY GLAND 8 [hp_X]/mL GOLD 10 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-8168-1 Scorodite Prunus 10 in 1 BOX LIQUID 10 4 48951-8168-1 Scorodite Prunus 1 mL in 1 AMPULE LIQUID 1 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8168 SCORODITE PRUNUS LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20250121_33bc061d-3767-4e71-b4ac-b8c8da2b0fd9.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-8168-1 48951816801 10 AMPULE in 1 BOX (48951-8168-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current