Home FDA labels f967d18c-e2ff-471e-9769-9f00242f9b0e Jet Lag 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 Jet Lag
Generic name ANACARDIUM ORIENTALE, APIS MELLIFICA, CARBO VEGETABILIS, CARDUUS MARIANUS, COCCULUS INDICUS, KALI PHOSPHORICUM, NUX VOMICA, PASSIFLORA INCARNATA, PHOSPHORICUM ACIDUM, TABACUM,
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 2bb38633-95a8-4db2-b4e8-8fc2fdbb5221
SPL ID f967d18c-e2ff-471e-9769-9f00242f9b0e
Version 6
Effective date 2024-05-20
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 05:56:45 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Jet Lag openfda.brand_name generic name ANACARDIUM ORIENTALE, APIS MELLIFICA, CARBO VEGETABILIS, CARDUUS MARIANUS, COCCULUS INDICUS, KALI PHOSPHORICUM, NUX VOMICA, PASSIFLORA INCARNATA, PHOSPHORICUM ACIDUM, TABACUM, openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0032-1 openfda.package_ndc ndc package 50845-0032-2 openfda.package_ndc ndc product 50845-0032 openfda.product_ndc ndc11 package 50845003201 derived:openfda.package_ndc ndc11 package 50845003202 derived:openfda.package_ndc spl id f967d18c-e2ff-471e-9769-9f00242f9b0e id spl set id 2bb38633-95a8-4db2-b4e8-8fc2fdbb5221 set_id unii 2P3VWU3H10 openfda.unii unii CI71S98N1Z openfda.unii unii 269XH13919 openfda.unii unii 6YR2608RSU openfda.unii unii U946SH95EE openfda.unii unii 810258W28U openfda.unii unii E4GA8884NN openfda.unii unii Y0F0BU8RDU openfda.unii unii 7S82P3R43Z openfda.unii unii CLF5YFS11O 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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist for more than 7 days, worsen, or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast-feeding, ask a doctor before using product. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken. Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.