Home FDA labels 0e7729de-1053-e578-e063-6394a90a7de6 W04 NEUROCALM 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 W04 NEUROCALM
Generic name AMERICAN GINSENG, AVENA SATIVA, CHAMOMILLA, COFFEA TOSTA, ESCHSCHOLTZIA CALIFORNICA, GLYCYRRHIZA GLABRA, HUMULUS LUPULUS, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, PASSIFLORA INCARNATA, PHOSPHORUS, PULSATILLA VULGARIS, VALERIANA OFFICINALIS, ZINCUM VALERIANICUM
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bf50b27a-e6d0-5393-e053-2995a90a1dff
SPL ID 0e7729de-1053-e578-e063-6394a90a7de6
Version 2
Effective date 2024-01-08
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 05:19:35 Harmonized routes table Harmonized routes SUBLINGUAL
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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name W04 NEUROCALM openfda.brand_name generic name AMERICAN GINSENG, AVENA SATIVA, CHAMOMILLA, COFFEA TOSTA, ESCHSCHOLTZIA CALIFORNICA, GLYCYRRHIZA GLABRA, HUMULUS LUPULUS, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, PASSIFLORA INCARNATA, PHOSPHORUS, PULSATILLA VULGARIS, VALERIANA OFFICINALIS, ZINCUM VALERIANICUM openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-2304-1 openfda.package_ndc ndc product 63479-2304 openfda.product_ndc ndc11 package 63479230401 derived:openfda.package_ndc spl id 0e7729de-1053-e578-e063-6394a90a7de6 id spl set id bf50b27a-e6d0-5393-e053-2995a90a1dff set_id unii 27YLU75U4W openfda.unii unii 9H58JRT35E openfda.unii unii MN0RX54EQA openfda.unii unii CI71S98N1Z openfda.unii unii XK4IUX8MNB openfda.unii unii 2788Z9758H openfda.unii unii 8W75VCV53Q openfda.unii unii 9315HN272X openfda.unii unii JWF5YAW3QW openfda.unii unii 01G73H6H83 openfda.unii unii MA9CQJ3F7F openfda.unii unii CLF5YFS11O openfda.unii unii G0R4UBI2ZZ openfda.unii unii I76KB35JEV 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: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if nervous irritability, restlessness, headache, anxiety, sweet craving, or other symptoms do not improve within 7 days or are accompanied by fever.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.