Home FDA labels b5a38025-d7f8-4589-9c07-553bdca09e1f Insomnia 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 Insomnia
Generic name AQUILEGIA VULGARIS, AVENA SATIVA, CHAMOMILLA, COFFEA CRUDA, CYPRIPEDIUM PUBESCENS, HUMULUS LUPULUS, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, MELATONIN, MELISSA OFFICINALIS, NATRUM MURIATICUM, PASSIFLORA INCARNATA, VALERIANA OFFICINALIS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 18c15f17-1a16-4595-9d23-20353363cd72
SPL ID b5a38025-d7f8-4589-9c07-553bdca09e1f
Version 2
Effective date 2023-10-31
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 06:28:10 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Insomnia openfda.brand_name generic name AQUILEGIA VULGARIS, AVENA SATIVA, CHAMOMILLA, COFFEA CRUDA, CYPRIPEDIUM PUBESCENS, HUMULUS LUPULUS, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, MELATONIN, MELISSA OFFICINALIS, NATRUM MURIATICUM, PASSIFLORA INCARNATA, VALERIANA OFFICINALIS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0272-2 openfda.package_ndc ndc package 50845-0272-1 openfda.package_ndc ndc product 50845-0272 openfda.product_ndc ndc11 package 50845027201 derived:openfda.package_ndc ndc11 package 50845027202 derived:openfda.package_ndc spl id b5a38025-d7f8-4589-9c07-553bdca09e1f id spl set id 18c15f17-1a16-4595-9d23-20353363cd72 set_id unii CI71S98N1Z openfda.unii unii XK4IUX8MNB openfda.unii unii YF70189L0N openfda.unii unii 3SW678MX72 openfda.unii unii 451W47IQ8X openfda.unii unii 8POZ61U1G2 openfda.unii unii JWF5YAW3QW openfda.unii unii 01G73H6H83 openfda.unii unii MA9CQJ3F7F openfda.unii unii CLF5YFS11O openfda.unii unii G0R4UBI2ZZ openfda.unii unii JL5DK93RCL openfda.unii unii 21Y9GZ1LZA 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: See box. 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.