Home FDA labels 0e76cbc6-8d03-7dc8-e063-6294a90a815a F14 INCDNT-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 F14 INCDNT-RLS
Generic name ARNICA MONTANA, ARNICA MONTANA, CALOCHORTUS GUNNISONII, CHERRY PLUM, CLEMATIS VITALBA, DICENTRA FORMOSA, EHRENDORFERIA CHRYSANTHA, ENGLISH HAWTHRON, HYPERICUM PERFORATUM, IGNATIA AMARA, IMPATIENS GLANDULIFERA, ORNITHOGALUM UMBELLATUM, PRUNELLA VULGARIS, ROCKROSE, RUTA GRAVEOLENS, STAPHYSAGRIA
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bf517ae5-84e8-5e7e-e053-2a95a90af220
SPL ID 0e76cbc6-8d03-7dc8-e063-6294a90a815a
Version 3
Effective date 2024-01-08
Source export date 2026-09-28
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:37:16 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 F14 INCDNT-RLS openfda.brand_name generic name ARNICA MONTANA, ARNICA MONTANA, CALOCHORTUS GUNNISONII, CHERRY PLUM, CLEMATIS VITALBA, DICENTRA FORMOSA, EHRENDORFERIA CHRYSANTHA, ENGLISH HAWTHRON, HYPERICUM PERFORATUM, IGNATIA AMARA, IMPATIENS GLANDULIFERA, ORNITHOGALUM UMBELLATUM, PRUNELLA VULGARIS, ROCKROSE, RUTA GRAVEOLENS, STAPHYSAGRIA openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0614-1 openfda.package_ndc ndc product 63479-0614 openfda.product_ndc ndc11 package 63479061401 derived:openfda.package_ndc spl id 0e76cbc6-8d03-7dc8-e063-6294a90a815a id spl set id bf517ae5-84e8-5e7e-e053-2a95a90af220 set_id unii 0KD7R09EAS openfda.unii unii XK4IUX8MNB openfda.unii unii 7SCP4N87CI openfda.unii unii 6OFG7K362R openfda.unii unii 00543AP1JV openfda.unii unii O80TY208ZW openfda.unii unii AT1FD041EF openfda.unii unii CZD6M4PY4B openfda.unii unii N94C2U587S openfda.unii unii 1NM3M2487K openfda.unii unii 51BRR32WPP openfda.unii unii AJU5O1A5ZV openfda.unii unii 68HKD4QMJR openfda.unii unii NT52AMP29J openfda.unii unii OZ0E5Y15PZ openfda.unii unii A6V4CUE7PV openfda.unii unii H4ORZ75P00 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 anguish, grief, restlessness,mental & physical trauma, or other 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.