Home FDA labels 0626ed57-c6fc-49dc-a8fa-e94033c0a914 Bio Detox Formula 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 Bio Detox Formula
Generic name EUCALYPTUS GLOBULUS, ALOE, HYDRASTIS CANADENSIS, ALLIUM SATIVUM, ALTERNARIA TENUIS NEES, ASPERGILLUS NIGER, BACILLUS TETANI, PNEUMOCOCCINUM, STAPHYLOCOCCUS AUREUS, STREPTOCOCCUS VIRIDANS, STAPHYSAGRIA, EUCALYPTOL, PYROGENIUM, LAC CANINUM, LAC VACCINUM, PESTINUM
Manufacturer Nutritional Specialties, Inc.
Product type HUMAN OTC DRUG
SPL set ID a4644c7a-fa08-4a43-909a-13b2be773e4e
SPL ID 0626ed57-c6fc-49dc-a8fa-e94033c0a914
Version 1
Effective date 2023-10-09
Source export date 2026-09-28
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:55:52 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Bio Detox Formula openfda.brand_name generic name EUCALYPTUS GLOBULUS, ALOE, HYDRASTIS CANADENSIS, ALLIUM SATIVUM, ALTERNARIA TENUIS NEES, ASPERGILLUS NIGER, BACILLUS TETANI, PNEUMOCOCCINUM, STAPHYLOCOCCUS AUREUS, STREPTOCOCCUS VIRIDANS, STAPHYSAGRIA, EUCALYPTOL, PYROGENIUM, LAC CANINUM, LAC VACCINUM, PESTINUM openfda.generic_name manufacturer name Nutritional Specialties, Inc. openfda.manufacturer_name ndc package 83027-0117-1 openfda.package_ndc ndc product 83027-0117 openfda.product_ndc ndc11 package 83027011701 derived:openfda.package_ndc spl id 0626ed57-c6fc-49dc-a8fa-e94033c0a914 id spl set id a4644c7a-fa08-4a43-909a-13b2be773e4e set_id unii V1V998DC17 openfda.unii unii 917J3173FT openfda.unii unii 00543AP1JV openfda.unii unii 751E8J54VM openfda.unii unii S6JJH3XV1D openfda.unii unii G39P120JQT openfda.unii unii 29SUH5R3HU openfda.unii unii O478WX4004 openfda.unii unii V5VD430YW9 openfda.unii unii ZW3Z11D0JV openfda.unii unii 52B29REC7H openfda.unii unii NNV2379HKR openfda.unii unii RV6J6604TK openfda.unii unii BT6U234YR2 openfda.unii unii 9IOA40ANG6 openfda.unii unii S546YLW6E6 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: Professional Use Only If pregnant or breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. If condition worsens, seek medical attention. KEEP OUT OF REACH OF CHILDREN Do not use if tamper evident seal is broken or missing. Store in a cool place after opening
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.