Home FDA labels 930a8c2f-6dcc-4179-8cc1-0724922b5d01 Pollen Distress 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 Pollen Distress
Generic name ALLIUM CEPA, APIS MELLIFICA, ARALIA RACEMOSA, ARUNDO MAURITANICA, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, RHUS TOX, SABADILLA, SANGUINARIA CANADENSIS, URTICA URENS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 034fcd90-81f7-4597-b58b-e2ed7047f6bd
SPL ID 930a8c2f-6dcc-4179-8cc1-0724922b5d01
Version 1
Effective date 2026-01-26
Source export date 2026-10-12
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 03:12:59 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Pollen Distress openfda.brand_name generic name ALLIUM CEPA, APIS MELLIFICA, ARALIA RACEMOSA, ARUNDO MAURITANICA, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, RHUS TOX, SABADILLA, SANGUINARIA CANADENSIS, URTICA URENS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0284-1 openfda.package_ndc ndc package 50845-0284-2 openfda.package_ndc ndc product 50845-0284 openfda.product_ndc ndc11 package 50845028401 derived:openfda.package_ndc ndc11 package 50845028402 derived:openfda.package_ndc spl id 930a8c2f-6dcc-4179-8cc1-0724922b5d01 id spl set id 034fcd90-81f7-4597-b58b-e2ed7047f6bd set_id unii C9642I91WL openfda.unii unii 3POA0Q644U openfda.unii unii T90W4582DU openfda.unii unii 639KR60Q1Q openfda.unii unii IHN2NQ5OF9 openfda.unii unii 6IO182RP7A openfda.unii unii VB06AV5US8 openfda.unii unii 6NAF1689IO openfda.unii unii 492225Q21H openfda.unii unii 5EF0HWI5WU openfda.unii unii 7S82P3R43Z openfda.unii unii ZXE7LB03WC openfda.unii unii N9288CD508 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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist for more than 7 days, worsen, or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a health professional before use. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken. Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.