Home FDA labels bdfbe914-ba46-48a2-885f-a5c8b74c8f7b Melatonin Pro 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 Melatonin Pro
Generic name CALCAREA CARBONICA, CHAMOMILLA, COCCULUS INDICUS, COFFEA CRUDA, FERRUM PHOSPHORICUM, KALI PHOSPHORICUM, MAGNESIA CARBONICA, MELATONIN, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (PRATENSIS)
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 1f374642-83f7-4e64-b330-0f6ef21000a9
SPL ID bdfbe914-ba46-48a2-885f-a5c8b74c8f7b
Version 4
Effective date 2023-07-19
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:34 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 · 19 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Melatonin Pro openfda.brand_name generic name CALCAREA CARBONICA, CHAMOMILLA, COCCULUS INDICUS, COFFEA CRUDA, FERRUM PHOSPHORICUM, KALI PHOSPHORICUM, MAGNESIA CARBONICA, MELATONIN, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (PRATENSIS) openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0500-1 openfda.package_ndc ndc product 44911-0500 openfda.product_ndc ndc11 package 44911050001 derived:openfda.package_ndc spl id bdfbe914-ba46-48a2-885f-a5c8b74c8f7b id spl set id 1f374642-83f7-4e64-b330-0f6ef21000a9 set_id unii CI71S98N1Z openfda.unii unii 269XH13919 openfda.unii unii 3SW678MX72 openfda.unii unii 451W47IQ8X openfda.unii unii 0E53J927NA openfda.unii unii 2E32821G6I openfda.unii unii 91GQH8I5F7 openfda.unii unii 8E272251DI openfda.unii unii 810258W28U openfda.unii unii G0R4UBI2ZZ openfda.unii unii JL5DK93RCL 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: Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place. Not to be taken by pregnant or lactating women. If you are taking MAO inhibitors, immunosuppressant drugs, anti-coagulation therapy, or anti-hypertensive medication, or have an autoimmune, seizure, psychiatric or depressive disorder consult your healthcare professional before using this product. Long-term use of melatonin has not been studied. May cause drowsiness. Do not use before or while operating a motor vehicle or heavy machinery.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.