Home NDC 53645-2001 Drosera
Product NDC 53645-2001
11-digit product format 536452001
Labeler code 53645
Product ID 53645-2001_fe921a82-8032-f0fd-e053-6394a90af4af
Type HUMAN OTC DRUG
Nonproprietary name Drosera
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-06-20
Substance DROSERA INTERMEDIA
Active strength 6 [hp_X]/55mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Drosera
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DROSERA INTERMEDIA 6 [hp_X]/55mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination B3G4A96QLY 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 53645-2001-3 Drosera 55 mL in 1 BOTTLE LIQUID 55 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53645-2001 DROSERA LIQUID [TRUE BOTANICA, LLC] 1 Current NDC, 1 package rows 20230710_fe91eee6-e240-64b7-e053-6394a90a4cf6.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 53645-2001-3 53645200103 55 mL in 1 BOTTLE (53645-2001-3) 55 ml 2023-06-20 No No Current