Home NDC 53645-2510 Acer Radix-Cinis 20X
Product NDC 53645-2510
11-digit product format 536452510
Labeler code 53645
Product ID 53645-2510_42ef6ff6-9d2a-71d6-e063-6294a90a219f
Type HUMAN OTC DRUG
Nonproprietary name Acer Radix-Cinis 20X
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-12-02
Substance ACER RUBRUM WHOLE
Active strength 20 [hp_X]/30mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Acer Radix-Cinis 20X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACER RUBRUM 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 W92E149717 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 53645-2510-6 Acer 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 53645-2510-6 53645251006 30 mL in 1 BOTTLE (53645-2510-6) 30 ml 2025-12-02 No No Current