Home NDC 48951-9306 Viscum Abietis 50
Product NDC 48951-9306
11-digit product format 489519306
Labeler code 48951
Product ID 48951-9306_44864fbf-46dd-478e-e063-6294a90ab98d
Type HUMAN OTC DRUG
Nonproprietary name Viscum Abietis 50
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 48951-9306-1 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 48951-9306-1 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 48951-9306-1 557ba5c1ecfa…9c80585c8c6e…
Additional Listing Data#
Finished product Yes
Brand name base Viscum Abietis 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VISCUM ALBUM FRUITING TOP 1 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination BK9092J5MP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-9306-1 Viscum Abietis 50 8 in 1 BOX LIQUID 8 10 48951-9306-1 Viscum Abietis 50 1 mL in 1 AMPULE LIQUID 1 10
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-9306 VISCUM ABIETIS 50 LIQUID [URIEL PHARMACY INC.] 9 Current NDC, Legacy NDC, 2 package rows 20241116_70b9dffb-a98b-4810-8ee8-af30fd4a0b73.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-9306-1 48951930601 8 AMPULE in 1 BOX (48951-9306-1) / 1 mL in 1 AMPULE 8 ampule 2014-08-01 0000-00-00 No No Current