Home FDA labels 11230476-2e97-4248-a7da-be620decae45 BioTox Bac 3 openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name BioTox Bac 3
Generic 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
Manufacturer The Wellness Center for Research and Education, Inc.
Product type HUMAN OTC DRUG
SPL set ID 29f1cba2-0bb6-43bf-a630-afc8fcb1ec81
SPL ID 11230476-2e97-4248-a7da-be620decae45
Version 2
Effective date 2025-06-06
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:36 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 19 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name BioTox Bac 3 openfda.brand_name generic 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 openfda.generic_name manufacturer name The Wellness Center for Research and Education, Inc. openfda.manufacturer_name ndc package 50181-0078-1 openfda.package_ndc ndc product 50181-0078 openfda.product_ndc ndc11 package 50181007801 derived:openfda.package_ndc spl id 11230476-2e97-4248-a7da-be620decae45 id spl set id 29f1cba2-0bb6-43bf-a630-afc8fcb1ec81 set_id unii UTX536WN6N openfda.unii unii 11E6VI8VEG openfda.unii unii 1NT28V9397 openfda.unii unii 4D7G21HDBC openfda.unii unii XH0F4IP2RX openfda.unii unii IX56B2GQX6 openfda.unii unii TJR6ZFY0F0 openfda.unii unii JQE470FAD0 openfda.unii unii OO358E3009 openfda.unii unii BT6U234YR2 openfda.unii unii 514B9K0L10 openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.