Home FDA labels f38a3cc8-c70a-4b30-a7ea-db1055902a16 Sleep Aid 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 Sleep Aid
Generic name ACONITUM NAPELLUS, AESCULUS HIPPOCASTANUM, FLOS, ARSENICUM ALBUM, AVENA SATIVA, BELLADONNA, CAMPHORA, CINCHONA OFFICINALIS, COFFEA CRUDA, CYPRIPEDIUM PUBESCENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI PHOSPHORICUM, PASSIFLORA INCARNATA, PHOSPHORUS, PULSATILLA, AND VALERIANA OFFICINALIS.
Manufacturer King Bio Inc.
Product type HUMAN OTC DRUG
SPL set ID 794b7e4f-b084-4aee-8c07-96bac459d698
SPL ID f38a3cc8-c70a-4b30-a7ea-db1055902a16
Version 1
Effective date 2026-03-04
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:51 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 Sleep Aid openfda.brand_name generic name ACONITUM NAPELLUS, AESCULUS HIPPOCASTANUM, FLOS, ARSENICUM ALBUM, AVENA SATIVA, BELLADONNA, CAMPHORA, CINCHONA OFFICINALIS, COFFEA CRUDA, CYPRIPEDIUM PUBESCENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI PHOSPHORICUM, PASSIFLORA INCARNATA, PHOSPHORUS, PULSATILLA, AND VALERIANA OFFICINALIS. openfda.generic_name manufacturer name King Bio Inc. openfda.manufacturer_name ndc package 57955-9986-2 openfda.package_ndc ndc product 57955-9986 openfda.product_ndc ndc11 package 57955998602 derived:openfda.package_ndc spl id f38a3cc8-c70a-4b30-a7ea-db1055902a16 id spl set id 794b7e4f-b084-4aee-8c07-96bac459d698 set_id unii 27YLU75U4W openfda.unii unii CI71S98N1Z openfda.unii unii KK0Z92II8M openfda.unii unii 3SW678MX72 openfda.unii unii 1NM3M2487K openfda.unii unii 4WRK2153H3 openfda.unii unii S7V92P67HO openfda.unii unii N20HL7Q941 openfda.unii unii S003A158SB openfda.unii unii WQZ3G9PF0H openfda.unii unii JWF5YAW3QW openfda.unii unii U0NQ8555JD openfda.unii unii MA9CQJ3F7F openfda.unii unii CLF5YFS11O openfda.unii unii I76KB35JEV 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 Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding, ask a healthcare professional before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.