Home FDA labels 55f5a7d5-3d34-498a-ba58-9de044037617 Elimitone 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 Elimitone
Generic name BELLIS PERENNIS, ECHINACEA (ANGUSTIFOLIA), TRIFOLIUM PRATENSE, PHYTOLACCA DECANDRA, ARNICA MONTANA, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, CALCAREA IODATA, KALI MURIATICUM, NITRICUM ACIDUM, PHOSPHORICUM ACIDUM, SULPHUR IODATUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID bc6352e0-6851-4971-948b-b18da7c1c8b6
SPL ID 55f5a7d5-3d34-498a-ba58-9de044037617
Version 3
Effective date 2024-10-24
Source export date 2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:28:13 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 Elimitone openfda.brand_name generic name BELLIS PERENNIS, ECHINACEA (ANGUSTIFOLIA), TRIFOLIUM PRATENSE, PHYTOLACCA DECANDRA, ARNICA MONTANA, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, CALCAREA IODATA, KALI MURIATICUM, NITRICUM ACIDUM, PHOSPHORICUM ACIDUM, SULPHUR IODATUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0490-1 openfda.package_ndc ndc product 44911-0490 openfda.product_ndc ndc11 package 44911049001 derived:openfda.package_ndc spl id 55f5a7d5-3d34-498a-ba58-9de044037617 id spl set id bc6352e0-6851-4971-948b-b18da7c1c8b6 set_id unii 11E6VI8VEG openfda.unii unii O80TY208ZW openfda.unii unii 411VRN1TV4 openfda.unii unii 2HU33I03UY openfda.unii unii VB06AV5US8 openfda.unii unii 660YQ98I10 openfda.unii unii RN2HC612GY openfda.unii unii E4GA8884NN openfda.unii unii 8EKI9QEE2H openfda.unii unii 4JS0838828 openfda.unii unii L6L8KA2AA0 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 breast-feeding, ask a health professional before use. 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. WARNING: Severe or persistent sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.