Viscum Abietis 1

Product NDC
48951-9301
11-digit product format
489519301
Labeler code
48951
Product ID
48951-9301_48884709-657a-6712-e063-6394a90a88e7
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Abietis 1
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-08-01
Substance
VISCUM ALBUM FRUITING TOP
Active strength
3 [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
Viscum Abietis 1
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VISCUM ALBUM FRUITING TOP3 [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
c9020643-a718-4709-aefd-ab02af6ec551Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9301-1Viscum Abietis 18 in 1 BOXLIQUID88
48951-9301-1Viscum Abietis 11 mL in 1 AMPULELIQUID18

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM ABIETIS 1MG LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM ABIETIS 1MG LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XVISCUM ABIETIS 1MG LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RVISCUM ABIETIS 1MG LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9301VISCUM ABIETIS 1 LIQUID [URIEL PHARMACY INC.]7Current NDC, Legacy NDC, 2 package rows20241116_c9020643-a718-4709-aefd-ab02af6ec551.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 1VISCUM ABIETIS 1Uriel Pharmacy Inc.c9020643-a718-4709-aefd-ab02af6ec5512026-01-16WarningsExact identifier
ndc (product): 48951-9301

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9301-1489519301018 AMPULE in 1 BOX (48951-9301-1) / 1 mL in 1 AMPULE8 ampule2014-08-010000-00-00NoNoCurrent