Home FDA labels b57f7b94-52ec-583c-e053-2995a90a8cbf Bact-In 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 Bact-In
Generic name ECHINACEA, HYDRASTIS CANADENSIS, IRIS VERSICOLOR, URTICA URENS, ACONITUM NAPELLUS, ARNICA MONTANA, ARSENICUM ALBUM, BAPTISIA TINCTORIA, BRYONIA, HYDRASTIS CANADENSIS, IODIUM, LACHESIS MUTUS, NUX VOMICA, PHOSPHORUS, PULSATILLA, RHUS TOXICODENDRON, ANTHRACINUM, PYROGENIUM
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 9a9f61c8-1913-1e6d-e053-2a95a90a8356
SPL ID b57f7b94-52ec-583c-e053-2995a90a8cbf
Version 2
Effective date 2020-12-02
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 05:56:48 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Bact-In openfda.brand_name generic name ECHINACEA, HYDRASTIS CANADENSIS, IRIS VERSICOLOR, URTICA URENS, ACONITUM NAPELLUS, ARNICA MONTANA, ARSENICUM ALBUM, BAPTISIA TINCTORIA, BRYONIA, HYDRASTIS CANADENSIS, IODIUM, LACHESIS MUTUS, NUX VOMICA, PHOSPHORUS, PULSATILLA, RHUS TOXICODENDRON, ANTHRACINUM, PYROGENIUM openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-4836-1 openfda.package_ndc ndc product 55714-4836 openfda.product_ndc ndc11 package 55714483601 derived:openfda.package_ndc spl id b57f7b94-52ec-583c-e053-2995a90a8cbf id spl set id 9a9f61c8-1913-1e6d-e053-2a95a90a8356 set_id unii 27YLU75U4W openfda.unii unii 269XH13919 openfda.unii unii O80TY208ZW openfda.unii unii 29SUH5R3HU openfda.unii unii 9679TC07X4 openfda.unii unii 41LZ22DD4N openfda.unii unii IHN2NQ5OF9 openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii 4N9P6CC1DX openfda.unii unii ZW3Z11D0JV openfda.unii unii T7J046YI2B openfda.unii unii VSW71SS07I openfda.unii unii U0NQ8555JD openfda.unii unii 5EF0HWI5WU openfda.unii unii X43D4L3DQC openfda.unii unii I76KB35JEV 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 SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.