Home FDA labels 49f473de-bd60-41e9-a4ef-9ade64f0c9de Drainpar 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 Drainpar
Generic name SOLIDAGO VIRGAUREA, TRIFOLIUM PRATENSE, PROPOLIS, HEPAR (SUIS), KIDNEY (SUIS), LYMPH NODE (SUIS), BERBERIS VULGARIS, BRYONIA (ALBA), CEANOTHUS AMERICANUS, CHELIDONIUM MAJUS, NUX VOMICA, SARSAPARILLA (SMILAX REGELII), TARAXACUM OFFICINALE
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 7e860080-eebf-43cb-957f-b2a17158a61b
SPL ID 49f473de-bd60-41e9-a4ef-9ade64f0c9de
Version 2
Effective date 2026-05-07
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 05:26:38 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 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Drainpar openfda.brand_name generic name SOLIDAGO VIRGAUREA, TRIFOLIUM PRATENSE, PROPOLIS, HEPAR (SUIS), KIDNEY (SUIS), LYMPH NODE (SUIS), BERBERIS VULGARIS, BRYONIA (ALBA), CEANOTHUS AMERICANUS, CHELIDONIUM MAJUS, NUX VOMICA, SARSAPARILLA (SMILAX REGELII), TARAXACUM OFFICINALE openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0704-1 openfda.package_ndc ndc product 44911-0704 openfda.product_ndc ndc11 package 44911070401 derived:openfda.package_ndc spl id 49f473de-bd60-41e9-a4ef-9ade64f0c9de id spl set id 7e860080-eebf-43cb-957f-b2a17158a61b set_id unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii 2H1576D5WG openfda.unii unii 1TH8Q20J0U openfda.unii unii 39981FM375 openfda.unii unii 33A7VYU29L openfda.unii unii X7BCI5P86H openfda.unii unii 6Y8XYV2NOF openfda.unii unii 25B1Y14T8N openfda.unii unii T7J046YI2B openfda.unii unii 5405K23S50 openfda.unii unii 4JS0838828 openfda.unii unii 6EC706HI7F 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 a 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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.