Home NDC 53645-1530-2 Lachesis Mutus
Product NDC 53645-1530
Requested package NDC 53645-1530-2
11-digit product format 536451530
Labeler code 53645
Product ID 53645-1530_fe1aaead-8e29-e1d4-e053-6394a90a96f4
Type HUMAN OTC DRUG
Nonproprietary name Lachesis Mutus
Dosage form GLOBULE
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2014-02-03
Substance LACHESIS MUTA VENOM
Active strength 30 [hp_X]/23g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Lachesis Mutus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LACHESIS MUTA VENOM 30 [hp_X]/23g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination VSW71SS07I Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53645-1530-2 Lachesis Mutus 23 g in 1 BOTTLE GLOBULE 23 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53645-1530 LACHESIS MUTUS GLOBULE [TRUE BOTANICA, LLC] 6 Current NDC, Legacy NDC, 1 package rows 20230621_61956c46-fd84-ce9d-e053-2991aa0af1fb.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 53645-1530-2 53645153002 23 g in 1 BOTTLE (53645-1530-2) 23 g 2014-02-03 No No Current