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
BOS TAURUS PITUITARY GLAND; CAMPHOR (NATURAL); FERROUS ARSENATE; GOLD; SLOE; VERATRUM ALBUM ROOT
Active strength
8; 4; 6; 10; 6; 4 [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

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Scorodite PrunusSCORODITE PRUNUSUriel Pharmacy Inc.33bc061d-3767-4e71-b4ac-b8c8da2b0fd92025-01-20WarningsExact identifier
ndc (product): 48951-8168

Additional Listing Data#

Finished product
Yes
Brand name base
Scorodite Prunus
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAMPHOR (NATURAL)8 [hp_X]/mL
VERATRUM ALBUM ROOT4 [hp_X]/mL
SLOE6 [hp_X]/mL
FERROUS ARSENATE10 [hp_X]/mL
BOS TAURUS PITUITARY GLAND6 [hp_X]/mL
GOLD4 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 6 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
N20HL7Q941Internal UNII lookup
QNS6W5US1ZInternal UNII lookup
3MLB4858X7Internal UNII lookup
129CO35H12Internal UNII lookup
7JM57I419KInternal UNII lookup
79Y1949PYOInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
33bc061d-3767-4e71-b4ac-b8c8da2b0fd9Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8168-1Scorodite Prunus10 in 1 BOXLIQUID104
48951-8168-1Scorodite Prunus1 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8168SCORODITE PRUNUS LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20250121_33bc061d-3767-4e71-b4ac-b8c8da2b0fd9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8168-14895181680110 AMPULE in 1 BOX (48951-8168-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent