Viscum Abietis 20

Product NDC
48951-9303
11-digit product format
489519303
Labeler code
48951
Product ID
48951-9303_448665ed-32c1-732c-e063-6394a90a6a56
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Abietis 20
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
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 20
Listing expiration
2026-12-31

Active Ingredients#

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

Harmonized Identifiers#

Field, Values table
FieldValues
UniiBK9092J5MP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9303-1Viscum Abietis 208 in 1 BOXLIQUID810
48951-9303-1Viscum Abietis 201 mL in 1 AMPULELIQUID110

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM ABIETIS 20MG LIQUID [URIEL PHARMACY INC.]2
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM ABIETIS 20MG LIQUID [URIEL PHARMACY INC.]2
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XVISCUM ABIETIS 20MG LIQUID [URIEL PHARMACY INC.]2
WATERINACTIVE INGREDIENT059QF0KO0RVISCUM ABIETIS 20MG LIQUID [URIEL PHARMACY INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9303VISCUM ABIETIS 20 LIQUID [URIEL PHARMACY INC.]9Current NDC, Legacy NDC, 2 package rows20241116_cb0aa68e-b296-44bb-9fc8-fe4fecabbd63.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9303-1489519303018 AMPULE in 1 BOX (48951-9303-1) / 1 mL in 1 AMPULE8 ampule2014-08-010000-00-00NoNoCurrent