Home FDA labels 2dd1fcbd-6eb5-f727-e063-6294a90a24c7 Just In Case 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 Just In Case
Generic name ACONITUM NAPELLUS, ARNICA MONTANA, BRYONIA, ECHINACEA, LEDUM PALUSTRE, ARSENICUM ALBUM, CENCHRIS CONTORTRIX, CROTALUS CASCAVELLA, CROTALUS HORRIDUS, LACHESIS MUTUS, MERCURIUS CORROSIVUS, NAJA TRIPUDIANS, PHOSPHORUS, TOXICOPHIS PUGNAX, VIPERA BERUS, ELAPS CORALLINUS, HELODERMA.
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID a035f2bf-2f5d-0a50-e053-2995a90a8d9c
SPL ID 2dd1fcbd-6eb5-f727-e063-6294a90a24c7
Version 2
Effective date 2025-02-10
Source export date 2026-09-28
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:28:05 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 Just In Case openfda.brand_name generic name ACONITUM NAPELLUS, ARNICA MONTANA, BRYONIA, ECHINACEA, LEDUM PALUSTRE, ARSENICUM ALBUM, CENCHRIS CONTORTRIX, CROTALUS CASCAVELLA, CROTALUS HORRIDUS, LACHESIS MUTUS, MERCURIUS CORROSIVUS, NAJA TRIPUDIANS, PHOSPHORUS, TOXICOPHIS PUGNAX, VIPERA BERUS, ELAPS CORALLINUS, HELODERMA. openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-2561-1 openfda.package_ndc ndc product 55714-2561 openfda.product_ndc ndc11 package 55714256101 derived:openfda.package_ndc spl id 2dd1fcbd-6eb5-f727-e063-6294a90a24c7 id spl set id a035f2bf-2f5d-0a50-e053-2995a90a8d9c set_id unii 27YLU75U4W openfda.unii unii 877L01IZ0P openfda.unii unii 2XF6I0446G openfda.unii unii O80TY208ZW openfda.unii unii X9V1Q8U150 openfda.unii unii O9M1UQ4YIO openfda.unii unii 53GH7MZT1R openfda.unii unii S7V92P67HO openfda.unii unii 0ORO6NCA4M openfda.unii unii 4N9P6CC1DX openfda.unii unii T7J046YI2B openfda.unii unii V0S6H36980 openfda.unii unii VSW71SS07I openfda.unii unii U0NQ8555JD openfda.unii unii ZZ4AG7L7VM openfda.unii unii YHA2XLJ956 openfda.unii unii 3BKX485ZP0 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.