Home NDC 0220-3029 Lachesis mutus
Product NDC 0220-3029
11-digit product format 002203029
Labeler code 0220
Product ID 0220-3029_0a0e30cc-ad7d-8cf3-e063-6394a90a974d
Type HUMAN OTC DRUG
Nonproprietary name LACHESIS MUTA VENOM
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance LACHESIS MUTA VENOM
Active strength 10 [hp_M]/10[hp_M]
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 10 [hp_M]/10[hp_M]
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 0220-3029-41 Lachesis mutus 10 [hp_M] in 1 TUBE PELLET 10 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-3029 LACHESIS MUTUS (LACHESIS MUTA VENOM ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20231114_861b7422-9b16-120e-e053-2991aa0aa91b.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 Marketing start Marketing end Sample Exclude flag Status 0220-3029-41 00220302941 10 [hp_M] in 1 TUBE (0220-3029-41) 1983-03-03 0000-00-00 No No Current