Home FDA labels 9f642fb4-0396-48c8-ba1e-e004e1ad0928 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 (BOVINE), HYDRASTIS CANADENSIS, ADRENALINUM, HISTAMINUM HYDROCHLORICUM, STICTA PULMONARIA
Manufacturer Nutritional Specialties, Inc.
Product type HUMAN OTC DRUG
SPL set ID f787b1ac-ab99-4e21-b0b7-caeb77b8744a
SPL ID 9f642fb4-0396-48c8-ba1e-e004e1ad0928
Version 1
Effective date 2026-02-23
Source export date 2026-09-28
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:56:02 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 (BOVINE), HYDRASTIS CANADENSIS, ADRENALINUM, HISTAMINUM HYDROCHLORICUM, STICTA PULMONARIA openfda.generic_name manufacturer name Nutritional Specialties, Inc. openfda.manufacturer_name ndc package 83027-0301-1 openfda.package_ndc ndc product 83027-0301 openfda.product_ndc ndc11 package 83027030101 derived:openfda.package_ndc spl id 9f642fb4-0396-48c8-ba1e-e004e1ad0928 id spl set id f787b1ac-ab99-4e21-b0b7-caeb77b8744a 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 ZW3Z11D0JV openfda.unii unii 7S82P3R43Z openfda.unii unii W8N8R55022 openfda.unii unii Z4B6561488 openfda.unii unii D1YM0P5Z2T 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: 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.