Home NDC 53645-2530 Quercus Radix-Cinis 20X
Product NDC 53645-2530
11-digit product format 536452530
Labeler code 53645
Product ID 53645-2530_44fe91ab-ee46-2a6d-e063-6394a90a029b
Type HUMAN OTC DRUG
Nonproprietary name Quercus Radix-Cinis 20X
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-12-02
Substance QUERCUS ALBA WHOLE
Active strength 20 [hp_X]/30mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Quercus Radix-Cinis 20X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength QUERCUS ALBA WHOLE 20 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8160EU25B5 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 53645-2530-6 Quercus Radix-Cinis 20X 30 mL in 1 BOTTLE LIQUID 30 1
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 53645-2530-6 53645253006 30 mL in 1 BOTTLE (53645-2530-6) 30 ml 2025-12-02 No No Current