Home FDA labels 92365727-70fe-4c1e-bac2-4d58a6948cd2 Lymphastat V 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 Lymphastat V
Generic name ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, HYDRASTIS CANADENSIS, SAMBUCUS NIGRA, ACONITUM NAPELLUS, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, INFLUENZINUM (2021-2022), LACHESIS MUTUS, RHUS TOX, PYROGENIUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 9ec6f663-5f15-4daf-a36b-49fbe1c53a6c
SPL ID 92365727-70fe-4c1e-bac2-4d58a6948cd2
Version 4
Effective date 2025-03-11
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 05:36:56 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Lymphastat V openfda.brand_name generic name ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, HYDRASTIS CANADENSIS, SAMBUCUS NIGRA, ACONITUM NAPELLUS, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, INFLUENZINUM (2021-2022), LACHESIS MUTUS, RHUS TOX, PYROGENIUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0657-1 openfda.package_ndc ndc product 44911-0657 openfda.product_ndc ndc11 package 44911065701 derived:openfda.package_ndc spl id 92365727-70fe-4c1e-bac2-4d58a6948cd2 id spl set id 9ec6f663-5f15-4daf-a36b-49fbe1c53a6c set_id unii V529EJB2CX openfda.unii unii 639KR60Q1Q openfda.unii unii VEH9U90EHX openfda.unii unii 29SUH5R3HU openfda.unii unii B93BQX9789 openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii VB06AV5US8 openfda.unii unii ZW3Z11D0JV openfda.unii unii 5329928G5N openfda.unii unii WQZ3G9PF0H openfda.unii unii T7J046YI2B openfda.unii unii RN2HC612GY openfda.unii unii VSW71SS07I openfda.unii unii U0NQ8555JD openfda.unii unii CT03BSA18U openfda.unii unii 1W0775VX6E openfda.unii unii WD5E5VYM2E 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: Sore throat warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by physician. Stop use and ask a doctor if symptoms persist for more than 2 days. 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. DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.