Home NDC 50181-0078-1 BioTox Bac
Product NDC 50181-0078
Requested package NDC 50181-0078-1
11-digit product format 501810078
Labeler code 50181
Product ID 50181-0078_11230476-2e97-4248-a7da-be620decae45
Type HUMAN OTC DRUG
Nonproprietary name Mycoplasma Pneumoniae, Proteus (Vulgaris), Candida Albicans, Colibacillinum Cum Natrum Muriaticum, Mycobacterium Paratuberculosis, Pasteurellosis (Pasteurella Multocida), Pneumococcinum, Thuja Occidentalis, Mycobacterium Avium Paratuberculosis, Phytolacca Decandra, Legionella Pneumophila, Shigella Sonnei
Dosage form LIQUID
Route ORAL
Labeler The Wellness Center for Research and Education, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-11-08
Marketing end 2026-12-09
Substance CANDIDA ALBICANS; ESCHERICHIA COLI; LEGIONELLA PNEUMOPHILA; MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS; MYCOPLASMA PNEUMONIAE; PASTEURELLA MULTOCIDA; PHYTOLACCA AMERICANA ROOT; PROTEUS INCONSTANS; SHIGELLA SONNEI; STREPTOCOCCUS PNEUMONIAE; THUJA OCCIDENTALIS LEAFY TWIG
Active strength 15; 15; 15; 15; 9; 15; 6; 12; 15; 15; 15 [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]
NDC exclude flag No
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 · 13 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base BioTox Bac
Brand name suffix 3 Active Ingredients# Ingredient, Strength table Ingredient Strength MYCOPLASMA PNEUMONIAE 15 [hp_X]/mL PROTEUS INCONSTANS 15 [hp_X]/mL CANDIDA ALBICANS 15 [hp_C]/mL ESCHERICHIA COLI 15 [hp_X]/mL MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS 9 [hp_X]/mL PASTEURELLA MULTOCIDA 15 [hp_X]/mL STREPTOCOCCUS PNEUMONIAE 6 [hp_C]/mL THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL PHYTOLACCA AMERICANA ROOT 15 [hp_C]/mL LEGIONELLA PNEUMOPHILA 15 [hp_X]/mL SHIGELLA SONNEI 15 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 matching rows.
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 50181-0078-1 BioTox Bac3 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50181-0078 BIOTOX BAC 3 (MYCOPLASMA PNEUMONIAE, PROTEUS (VULGARIS), CANDIDA ALBICANS, COLIBACILLINUM CUM NATRUM MURIATICUM, MYCOBACTERIUM PARATUBERCULOSIS, PASTEURELLOSIS (PASTEURELLA MULTOCIDA), PNEUMOCOCCINUM, THUJA OCCIDENTALIS, MYCOBACTERIUM AVIUM PARATUBERCULOSIS, PHYTOLACCA DECANDRA, LEGIONELLA PNEUMOPHILA, SHIGELLA SONNEI) LIQUID [THE WELLNESS CENTER FOR RESEARCH AND EDUCATION, INC.] 1 Current NDC, Legacy NDC, 1 package rows 20211109_29f1cba2-0bb6-43bf-a630-afc8fcb1ec81.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join BioTox Bac 3 MYCOPLASMA PNEUMONIAE, PROTEUS (VULGARIS), CANDIDA ALBICANS, COLIBACILLINUM CUM NATRUM MURIATICUM, MYCOBACTERIUM PARATUBERCULOSIS, PASTEURELLOSIS (PASTEURELLA MULTOCIDA), PNEUMOCOCCINUM, THUJA OCCIDENTALIS, MYCOBACTERIUM AVIUM PARATUBERCULOSIS, PHYTOLACCA DECANDRA, LEGIONELLA PNEUMOPHILA, SHIGELLA SONNEI The Wellness Center for Research and Education, Inc. 29f1cba2-0bb6-43bf-a630-afc8fcb1ec81 2025-06-06 Warnings Exact identifier ndc (package): 50181-0078-1 ndc (product): 50181-0078 ndc11 (package): 50181007801
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50181-0078-1 50181007801 30 mL in 1 BOTTLE, DROPPER (50181-0078-1) 30 ml 2021-11-08 2026-12-09 No No Current