FDA.reportPublic FDA data

Levico Prunus

Product NDC
48951-6026
Requested package NDC
48951-6026-1
11-digit product format
489516026
Labeler code
48951
Product ID
48951-6026_4bd386c3-bcc0-2d41-e063-6394a90a67b7
Type
HUMAN OTC DRUG
Nonproprietary name
Levico Prunus
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
FERRIC OXIDE RED; FERROUS ARSENATE; PRUNUS SPINOSA FLOWER BUD; ST. JOHN'S WORT
Active strength
6; 3; 6; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Levico Prunus
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ST. JOHN'S WORT6 [hp_X]/mL
FERROUS ARSENATE3 [hp_X]/mL
FERRIC OXIDE RED6 [hp_X]/mL
PRUNUS SPINOSA FLOWER BUD3 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
UFH8805FKAInternal UNII lookup
129CO35H12Internal UNII lookup
1K09F3G675Internal UNII lookup
53Y84VPS2WInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
63db9374-8ee2-48cf-8799-454c95869808Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-6026-12026-01-29C16284748780-149896155-ae64-586f-e063-e6dba90add90Levico Prunus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-6026-1Levico Prunus1 mL in 1 AMPULELIQUID15
48951-6026-1Levico Prunus10 in 1 BOXLIQUID105

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FERRIC OXIDE REDACTIVE INGREDIENT1K09F3G675LEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
FERROUS ARSENATEACTIVE INGREDIENT129CO35H12LEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
PRUNUS SPINOSA FLOWER BUDACTIVE INGREDIENT53Y84VPS2WLEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
ST. JOHN'S WORTACTIVE INGREDIENTUFH8805FKALEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
FERRIC OXIDE REDACTIVE MOIETY1K09F3G675LEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
FERROUS ARSENATEACTIVE MOIETY129CO35H12LEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
PRUNUS SPINOSA FLOWER BUDACTIVE MOIETY53Y84VPS2WLEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
ST. JOHN'S WORTACTIVE MOIETYUFH8805FKALEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XLEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RLEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-6026LEVICO PRUNUS LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20240312_63db9374-8ee2-48cf-8799-454c95869808.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Levico PrunusLEVICO PRUNUSUriel Pharmacy Inc.63db9374-8ee2-48cf-8799-454c958698082026-02-27WarningsExact identifier
ndc (package): 48951-6026-1
ndc (product): 48951-6026
ndc11 (package): 48951602601

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-6026-14895160260110 AMPULE in 1 BOX (48951-6026-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent