Helleborus e pl. tota 4

Product NDC
48951-5038
11-digit product format
489515038
Labeler code
48951
Product ID
48951-5038_6ccb8d0f-6c01-26ae-e053-2991aa0abeb8
Type
HUMAN OTC DRUG
Nonproprietary name
Helleborus e pl. tota 4
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
HELLEBORUS FOETIDUS ROOT
Active strength
4 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Additional Listing Data#

Finished product
Yes
Brand name base
Helleborus e pl. tota 4
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HELLEBORUS FOETIDUS ROOT4 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
332Y7EES96Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
462c4c00-8469-45d1-9029-2aa48b0f4af9Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-5038-1Helleborus e pl. tota 410 in 1 BOXLIQUID104
48951-5038-1Helleborus e pl. tota 41 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HELLEBORUS FOETIDUS ROOTACTIVE INGREDIENT332Y7EES96HELLEBORUS E PL. TOTA 4 LIQUID [URIEL PHARMACY INC.]1
HELLEBORUS FOETIDUS ROOTACTIVE MOIETY332Y7EES96HELLEBORUS E PL. TOTA 4 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XHELLEBORUS E PL. TOTA 4 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RHELLEBORUS E PL. TOTA 4 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-5038HELLEBORUS E PL. TOTA 4 LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20241218_462c4c00-8469-45d1-9029-2aa48b0f4af9.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
Helleborus e pl. tota 4HELLEBORUS E PL. TOTA 4Uriel Pharmacy Inc.462c4c00-8469-45d1-9029-2aa48b0f4af92026-06-16WarningsExact identifier
ndc (product): 48951-5038

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-5038-14895150380110 AMPULE in 1 BOX (48951-5038-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent