Viscum Abietis 100

Product NDC
48951-9307
11-digit product format
489519307
Labeler code
48951
Product ID
48951-9307_4395781f-e3bc-ec5d-e063-6394a90a00a7
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Abietis 100
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
VISCUM ALBUM FRUITING TOP
Active strength
1 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Viscum Abietis 100
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VISCUM ALBUM FRUITING TOP1 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
BK9092J5MPInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
41aea12a-e79c-45b0-9d2a-938f1d8bab67Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9307-1Viscum Abietis 1001 mL in 1 AMPULELIQUID110
48951-9307-1Viscum Abietis 1008 in 1 BOXLIQUID810

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM ABIETIS 100MG LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM ABIETIS 100MG LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XVISCUM ABIETIS 100MG LIQUID [URIEL PHARMACY INC.]1
WATER BUFFALOINACTIVE INGREDIENT0A4PW6CRAIVISCUM ABIETIS 100MG LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9307VISCUM ABIETIS 100 LIQUID [URIEL PHARMACY INC.]9Current NDC, Legacy NDC, 2 package rows20241207_41aea12a-e79c-45b0-9d2a-938f1d8bab67.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
Viscum Abietis 100VISCUM ABIETIS 100Uriel Pharmacy Inc.41aea12a-e79c-45b0-9d2a-938f1d8bab672025-11-14WarningsExact identifier
ndc (product): 48951-9307

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9307-1489519307018 AMPULE in 1 BOX (48951-9307-1) / 1 mL in 1 AMPULE8 ampule2014-08-010000-00-00NoNoCurrent