Carpellum Mali Comp.

Product NDC
48951-3034
11-digit product format
489513034
Labeler code
48951
Product ID
48951-3034_3b53dbfd-3a41-bee3-e063-6394a90a8e27
Type
HUMAN OTC DRUG
Nonproprietary name
Carpellum Mali Comp.
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ENGLISH WALNUT; MALUS DOMESTICA WHOLE
Active strength
4; 4 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Nut Proteins [EXT]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Carpellum Mali Comp.
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ENGLISH WALNUT4 [hp_X]/mL
MALUS DOMESTICA WHOLE4 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1V3SHR7QB7Internal UNII lookup
04W636S1V3Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
d6097ade-ed9c-4903-b0ea-c9424909d657Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3034-3Carpellum Mali Comp.60 mL in 1 BOTTLE, DROPPERLIQUID604

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ENGLISH WALNUTACTIVE INGREDIENT1V3SHR7QB7CARPELLUM MALI COMP. LIQUID [URIEL PHARMACY INC.]1
MALUS DOMESTICA WHOLEACTIVE INGREDIENT04W636S1V3CARPELLUM MALI COMP. LIQUID [URIEL PHARMACY INC.]1
ENGLISH WALNUTACTIVE MOIETY1V3SHR7QB7CARPELLUM MALI COMP. LIQUID [URIEL PHARMACY INC.]1
MALUS DOMESTICA WHOLEACTIVE MOIETY04W636S1V3CARPELLUM MALI COMP. LIQUID [URIEL PHARMACY INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MCARPELLUM MALI COMP. LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RCARPELLUM MALI COMP. LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3034CARPELLUM MALI COMP. LIQUID [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 1 package rows20180424_d6097ade-ed9c-4903-b0ea-c9424909d657.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
Carpellum Mali Comp.CARPELLUM MALI COMP.Uriel Pharmacy Inc.d6097ade-ed9c-4903-b0ea-c9424909d6572025-08-01WarningsExact identifier
ndc (product): 48951-3034

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3034-34895130340360 mL in 1 BOTTLE, DROPPER (48951-3034-3) 60 ml2009-09-010000-00-00NoNoCurrent