Home FDA labels 0e76f50e-2564-d499-e063-6394a90aa92e F08 FRGV 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 F08 FRGV
Generic name ALLEGHENY MONKEYFLOWER, ARNICA MONTANA, ARNICA MONTANA FLOWER, CEANOTHUS INTEGERRIMUS, EHRENDORFERIA CHRYSANTHA, FAGUS SYLVATICA FLOWER, IGNATIA AMARA, ILEX AQUIFOLIUM FLOWER, MALUS SYLVESTRIS FLOWER, MULLEIN FLOWER, NETTLELEAF GIANT HYSSOP, PINUS SYLVESTRIS FLOWER, SALIX ALBA FLOWER
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bc91d5bd-fa6e-8245-e053-2995a90a3e8c
SPL ID 0e76f50e-2564-d499-e063-6394a90aa92e
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 05:15:22 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 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name F08 FRGV openfda.brand_name generic name ALLEGHENY MONKEYFLOWER, ARNICA MONTANA, ARNICA MONTANA FLOWER, CEANOTHUS INTEGERRIMUS, EHRENDORFERIA CHRYSANTHA, FAGUS SYLVATICA FLOWER, IGNATIA AMARA, ILEX AQUIFOLIUM FLOWER, MALUS SYLVESTRIS FLOWER, MULLEIN FLOWER, NETTLELEAF GIANT HYSSOP, PINUS SYLVESTRIS FLOWER, SALIX ALBA FLOWER openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0608-1 openfda.package_ndc ndc product 63479-0608 openfda.product_ndc ndc11 package 63479060801 derived:openfda.package_ndc spl id 0e76f50e-2564-d499-e063-6394a90aa92e id spl set id bc91d5bd-fa6e-8245-e053-2995a90a3e8c set_id unii XBP5X7E70R openfda.unii unii 2HEM73YI9I openfda.unii unii 6ZJ8N1924Z openfda.unii unii O80TY208ZW openfda.unii unii 5ENR9SAN1W openfda.unii unii N7FC535Q3R openfda.unii unii N76K76PTFU openfda.unii unii 1NM3M2487K openfda.unii unii 8A94843BM7 openfda.unii unii 21AF0IHY5U openfda.unii unii 68HKD4QMJR openfda.unii unii OZ0E5Y15PZ openfda.unii unii W4KH5N2DCK 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, resentfulness, anger, combativeness, 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.