Home FDA labels 3602f83f-033b-4c57-8769-3e57782429e5 Influenseg 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 Influenseg
Generic name GELSEMIUM SEMPERVIRENS, SAMBUCUS NIGRA, GALPHIMIA GLAUCA, CAUSTICUM, EUPATORIUM PERFOLIATUM, IPECACUANHA, ACONITUM NAPELLUS, KALI BICHROMICUM, AVENA SATIVA, INFLUENZINUM (2024-2025), LOBELIA PURPURESCENS, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ECHINACEA (ANGUSTIFOLIA), CANCHALAGUA
Manufacturer Nucleic Products, LLC
Product type HUMAN OTC DRUG
SPL set ID 6d673ec9-fdb3-48a0-9a4f-bb65e290f9a4
SPL ID 3602f83f-033b-4c57-8769-3e57782429e5
Version 1
Effective date 2026-02-27
Source export date 2026-09-28
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:28:00 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Influenseg openfda.brand_name generic name GELSEMIUM SEMPERVIRENS, SAMBUCUS NIGRA, GALPHIMIA GLAUCA, CAUSTICUM, EUPATORIUM PERFOLIATUM, IPECACUANHA, ACONITUM NAPELLUS, KALI BICHROMICUM, AVENA SATIVA, INFLUENZINUM (2024-2025), LOBELIA PURPURESCENS, ANAS BARBARIAE, HEPATIS ET CORDIS EXTRACTUM, ECHINACEA (ANGUSTIFOLIA), CANCHALAGUA openfda.generic_name manufacturer name Nucleic Products, LLC openfda.manufacturer_name ndc package 75053-0100-1 openfda.package_ndc ndc product 75053-0100 openfda.product_ndc ndc11 package 75053010001 derived:openfda.package_ndc spl id 3602f83f-033b-4c57-8769-3e57782429e5 id spl set id 6d673ec9-fdb3-48a0-9a4f-bb65e290f9a4 set_id unii PS2DCE2WVF openfda.unii unii DD5FO1WKFU openfda.unii unii 93PH5Q8M7E openfda.unii unii H93GMC21MW openfda.unii unii 639KR60Q1Q openfda.unii unii 901NKD188B openfda.unii unii AU5C98U4BB openfda.unii unii VB06AV5US8 openfda.unii unii CYK5P89K8X openfda.unii unii 62I3C8233L openfda.unii unii RN2HC612GY openfda.unii unii U0NQ8555JD openfda.unii unii T4423S18FM openfda.unii unii CT03BSA18U openfda.unii unii MA9CQJ3F7F openfda.unii unii 1W0775VX6E openfda.unii unii 6TU4EY6UNW 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: As with any drug, ask a doctor before use if pregnant or nursing. Consult a physician if: Symptoms persist for more than 7 days or worsen Keep this and all medications out of the reach of children. In case of accidental overdose, contact a medical professional or a poison control center immediately. Do not use if seal is broken or missing. This Product does not contain sugar, starch, preservatives, artificial flavors or additives, and no wheat, gluten, soy, or milk derivatives.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.