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: a05f7d34-9f5c-42a4-a9f5-8e62e1e86020
SPL ID: 1858a1f0-ba02-4fd0-af56-0673e0b4af17
Version: 5
Effective date: 2025-11-20
Source export date: 2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:46:28

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	50845-0270-1	openfda.package_ndc
ndc	package	50845-0270-2	openfda.package_ndc
ndc	product	50845-0270	openfda.product_ndc
ndc11	package	50845027001	derived:openfda.package_ndc
ndc11	package	50845027002	derived:openfda.package_ndc
spl id		1858a1f0-ba02-4fd0-af56-0673e0b4af17	id
spl set id		a05f7d34-9f5c-42a4-a9f5-8e62e1e86020	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 doctor before using product.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.