Home FDA labels a9693600-1d91-4274-b38b-b375649c8832 Pollen and Dander Liquescence 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 and Dander Liquescence
Generic name ALLIUM CEPA, EUPHRASIA OFFICINALIS, ECHINACEA (ANGUSTIFOLIA), SABADILLA, AMBROSIA ARTEMISIAEFOLIA, APIS MELLIFICA, GALIUM APARINE, GLANDULA SUPRARENALIS (BOVINE), HEPAR SUIS, HYDRASTIS CANADENSIS, ADRENALINUM, EPHEDRA VULGARIS, HISTAMINUM HYDROCHLORICUM
Manufacturer Nutritional Specialties, Inc.
Product type HUMAN OTC DRUG
SPL set ID 395b8a0e-b718-4d6f-9b24-b80119b90348
SPL ID a9693600-1d91-4274-b38b-b375649c8832
Version 2
Effective date 2025-10-06
Source export date 2026-10-12
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:28:14 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 Pollen and Dander Liquescence openfda.brand_name generic name ALLIUM CEPA, EUPHRASIA OFFICINALIS, ECHINACEA (ANGUSTIFOLIA), SABADILLA, AMBROSIA ARTEMISIAEFOLIA, APIS MELLIFICA, GALIUM APARINE, GLANDULA SUPRARENALIS (BOVINE), HEPAR SUIS, HYDRASTIS CANADENSIS, ADRENALINUM, EPHEDRA VULGARIS, HISTAMINUM HYDROCHLORICUM openfda.generic_name manufacturer name Nutritional Specialties, Inc. openfda.manufacturer_name ndc package 83027-0058-1 openfda.package_ndc ndc product 83027-0058 openfda.product_ndc ndc11 package 83027005801 derived:openfda.package_ndc spl id a9693600-1d91-4274-b38b-b375649c8832 id spl set id 395b8a0e-b718-4d6f-9b24-b80119b90348 set_id unii C9642I91WL openfda.unii unii 3POA0Q644U openfda.unii unii YKH834O4BH openfda.unii unii VB06AV5US8 openfda.unii unii 9W34L2CQ9A openfda.unii unii M2776SWB29 openfda.unii unii 6NAF1689IO openfda.unii unii 492225Q21H openfda.unii unii R55VQ87DP3 openfda.unii unii ZW3Z11D0JV openfda.unii unii 7S82P3R43Z openfda.unii unii Z4B6561488 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: Professional Use Only If pregnant or breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. If condition worsens, seek medical attention. KEEP OUT OF REACH OF CHILDREN Do not use if tamper evident seal is broken or missing. Store in a cool place after opening
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.