Home FDA labels a0908260-6064-482b-879c-28d442a76cb1 V HP 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 V HP
Generic name ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), CARCINOSIN, ECHINACEA (ANGUSTIFOLIA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PYROGENIUM, RHUS TOX, SULPHUR
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID ea12ca3b-19e0-4d4a-9514-4d28d214e1e7
SPL ID a0908260-6064-482b-879c-28d442a76cb1
Version 2
Effective date 2026-06-12
Source export date 2026-09-28
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:26:35 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name V HP openfda.brand_name generic name ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), CARCINOSIN, ECHINACEA (ANGUSTIFOLIA), EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PYROGENIUM, RHUS TOX, SULPHUR openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0717-1 openfda.package_ndc ndc product 44911-0717 openfda.product_ndc ndc11 package 44911071701 derived:openfda.package_ndc spl id a0908260-6064-482b-879c-28d442a76cb1 id spl set id ea12ca3b-19e0-4d4a-9514-4d28d214e1e7 set_id unii 27YLU75U4W openfda.unii unii 639KR60Q1Q openfda.unii unii 29SUH5R3HU openfda.unii unii 451W47IQ8X openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii VB06AV5US8 openfda.unii unii C62OO7VD9K openfda.unii unii WQZ3G9PF0H openfda.unii unii T7J046YI2B openfda.unii unii 70FD1KFU70 openfda.unii unii RN2HC612GY openfda.unii unii E4GA8884NN openfda.unii unii 1W0775VX6E openfda.unii unii C88X29Y479 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 a 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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.