Home FDA labels 0e76e634-d944-70ac-e063-6294a90a6ad3 F03 FR-RLS 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 F03 FR-RLS
Generic name ASPEN, ARSENICUM ALBUM, DIPLACUS AURANTIACUS, GARLIC, LILIUM TIGRINUM, LOQUAT, LUFFA OPERCULATA, MIMULUS GUTTATUS, PENSTEMON DAVIDSONII, PRUNUS CERASIFERA, RED HORSE CHESTNUT, RUBUS URSINUS, ROCKROSE, TOXICODENDRON DIVERSILOBUM, VIOLA ODORATA, WATERMELON, YELLOW JASMINE
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bccede22-e48f-52bc-e053-2995a90a6d0f
SPL ID 0e76e634-d944-70ac-e063-6294a90a6ad3
Version 2
Effective date 2024-01-08
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:23 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name F03 FR-RLS openfda.brand_name generic name ASPEN, ARSENICUM ALBUM, DIPLACUS AURANTIACUS, GARLIC, LILIUM TIGRINUM, LOQUAT, LUFFA OPERCULATA, MIMULUS GUTTATUS, PENSTEMON DAVIDSONII, PRUNUS CERASIFERA, RED HORSE CHESTNUT, RUBUS URSINUS, ROCKROSE, TOXICODENDRON DIVERSILOBUM, VIOLA ODORATA, WATERMELON, YELLOW JASMINE openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0603-1 openfda.package_ndc ndc product 63479-0603 openfda.product_ndc ndc11 package 63479060301 derived:openfda.package_ndc spl id 0e76e634-d944-70ac-e063-6294a90a6ad3 id spl set id bccede22-e48f-52bc-e053-2995a90a6d0f set_id unii 0KD7R09EAS openfda.unii unii 192426I5JU openfda.unii unii 8K9DCX606Z openfda.unii unii 5Q01F7TPJJ openfda.unii unii 2FCJ9QNJ7O openfda.unii unii 9211E5735B openfda.unii unii 639KR60Q1Q openfda.unii unii X67Z2963PI openfda.unii unii 51BRR32WPP openfda.unii unii S7V92P67HO openfda.unii unii C4MO6809HU openfda.unii unii IIF21WT8O3 openfda.unii unii 438W01FC7A openfda.unii unii 231473QB6R openfda.unii unii 717DPT98VM openfda.unii unii TO6G4140YA openfda.unii unii EB3AN7DKSL 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 restlessness, fearfulness, backache, cold sweat, buzzing ears, weak memory, dizziness, 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.