Home NDC 53645-1832 Gelsemium 6X
Product NDC 53645-1832
11-digit product format 536451832
Labeler code 53645
Product ID 53645-1832_2f39e4b6-82b7-cf2a-e063-6294a90afb2e
Type HUMAN OTC DRUG
Nonproprietary name Gelsemium sempervirens
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-05-28
Substance GELSEMIUM SEMPERVIRENS ROOT
Active strength 6 [hp_X]/30mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Gelsemium 6X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 639KR60Q1Q 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 53645-1832-6 Gelsemium 6X 30 mL in 1 BOTTLE LIQUID 30 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 53645-1832-6 53645183206 30 mL in 1 BOTTLE (53645-1832-6) 30 ml 2025-05-28 No No Current