Home NDC 43857-0312 Toxodetox
Product NDC 43857-0312
11-digit product format 438570312
Labeler code 43857
Product ID 43857-0312_5f52b7e0-b9ee-4f2c-8b17-bbea9e72681f
Type HUMAN OTC DRUG
Nonproprietary name Toxoplasma Gondii
Dosage form LIQUID
Route ORAL
Labeler BioActive Nutritional, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2014-07-11
Substance TOXOPLASMA GONDII
Active strength 12 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Toxodetox
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOXOPLASMA GONDII 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination BMV90JF469 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 43857-0312-1 Toxodetox 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43857-0312 TOXODETOX (TOXOPLASMA GONDII) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20180626_36a8546e-926d-465b-9c7d-8544dacb8331.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 Marketing end Sample Exclude flag Status 43857-0312-1 43857031201 30 mL in 1 BOTTLE, DROPPER (43857-0312-1) 30 ml 2014-07-11 0000-00-00 No No Current