Home NDC 53645-2190 Viscum Populus RK 30X
Product NDC 53645-2190
11-digit product format 536452190
Labeler code 53645
Product ID 53645-2190_fbfda05e-2e21-1cc2-e053-6394a90a88bd
Type HUMAN OTC DRUG
Nonproprietary name Viscum Populus RK 30X
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-05-15
Substance VISCUM ALBUM WHOLE
Active strength 30 [hp_X]/20mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Viscum Populus RK 30X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VISCUM ALBUM WHOLE 30 [hp_X]/20mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination E6839Q6DO1 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 53645-2190-4 Viscum Populus RK 30X 20 mL in 1 BOTTLE LIQUID 20 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53645-2190 VISCUM POPULUS RK 30X LIQUID [TRUE BOTANICA, LLC] 1 Current NDC, 1 package rows 20230519_fbfd80e2-a697-c061-e053-6394a90a79ec.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 Sample Exclude flag Status 53645-2190-4 53645219004 20 mL in 1 BOTTLE (53645-2190-4) 20 ml 2023-05-15 No No Current