Home NDC 43857-0194 THYMUS
Product NDC 43857-0194
11-digit product format 438570194
Labeler code 43857
Product ID 43857-0194_7dc1fa07-add3-4e4b-81ee-39468dcf0e0c
Type HUMAN OTC DRUG
Nonproprietary name Thymus (Suis)
Dosage form LIQUID
Route ORAL
Labeler BioActive Nutrional, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2013-08-09
Substance SUS SCROFA THYMUS
Active strength 8 [hp_X]/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 43857-0194-1 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 43857-0194-1 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 43857-0194-1 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 43857-0194-1 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 43857-0194-1 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base THYMUS
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SUS SCROFA THYMUS 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7B69B0BD62 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 43857-0194-1 THYMUS 30 mL in 1 BOTTLE, SPRAY LIQUID 30 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43857-0194 THYMUS (THYMUS (SUIS)) LIQUID [BIOACTIVE NUTRIONAL, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20241020_efde66a6-0571-41b5-b854-58a89551173b.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 43857-0194-1 43857019401 30 mL in 1 BOTTLE, SPRAY (43857-0194-1) 30 ml 2016-12-06 0000-00-00 No No Current