Viscum Abietis 10

Product NDC
48951-9304
11-digit product format
489519304
Labeler code
48951
Product ID
48951-9304_4486c006-17e9-d796-e063-6294a90a64bc
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Abietis 10
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
2 [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 10
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VISCUM ALBUM FRUITING TOP2 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiBK9092J5MP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9304-1Viscum Abietis 101 mL in 1 AMPULELIQUID111
48951-9304-1Viscum Abietis 108 in 1 BOXLIQUID811

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM ABIETIS 10MG LIQUID [URIEL PHARMACY INC.]2
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM ABIETIS 10MG LIQUID [URIEL PHARMACY INC.]2
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XVISCUM ABIETIS 10MG LIQUID [URIEL PHARMACY INC.]2
WATERINACTIVE INGREDIENT059QF0KO0RVISCUM ABIETIS 10MG LIQUID [URIEL PHARMACY INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9304VISCUM ABIETIS 10 LIQUID [URIEL PHARMACY INC.]10Current NDC, Legacy NDC, 2 package rows20241116_70c0766a-3965-49bd-9d9e-e87a299b18ba.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9304-1489519304018 AMPULE in 1 BOX (48951-9304-1) / 1 mL in 1 AMPULE8 ampule2014-08-010000-00-00NoNoCurrent