Home FDA labels d46c8440-f512-4247-9eb0-8a7b4f165bb3 Allergen II 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 Allergen II
Generic name POTASSIUM GLUCONATE, ADRENALINUM, HEPAR BOVINE, ARSENICUM ALBUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SULPHUR, AMBROSIA ARTEMISIAEFOLIA, KENTUCKY BLUEGRASS, ORCHARD GRASS, BERMUDA GRASS, JOHNSON GRASS, RYE GRASS, VERNAL GRASS, BAHIA GRASS, TIMOTHY GRASS, HISTAMINUM HYDROCHLORICUM
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID 2140b105-60d6-4b52-82f5-407211fd6933
SPL ID d46c8440-f512-4247-9eb0-8a7b4f165bb3
Version 3
Effective date 2023-06-05
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:28:58 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 Allergen II openfda.brand_name generic name POTASSIUM GLUCONATE, ADRENALINUM, HEPAR BOVINE, ARSENICUM ALBUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SULPHUR, AMBROSIA ARTEMISIAEFOLIA, KENTUCKY BLUEGRASS, ORCHARD GRASS, BERMUDA GRASS, JOHNSON GRASS, RYE GRASS, VERNAL GRASS, BAHIA GRASS, TIMOTHY GRASS, HISTAMINUM HYDROCHLORICUM openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0557-1 openfda.package_ndc ndc product 43857-0557 openfda.product_ndc ndc11 package 43857055701 derived:openfda.package_ndc spl id d46c8440-f512-4247-9eb0-8a7b4f165bb3 id spl set id 2140b105-60d6-4b52-82f5-407211fd6933 set_id unii 27YLU75U4W openfda.unii unii YMW1K70E4Q openfda.unii unii 577VA5B4HP openfda.unii unii 3POA0Q644U openfda.unii unii 12H3K5QKN9 openfda.unii unii V003SHB7VK openfda.unii unii S7PW24BX20 openfda.unii unii J41552QKAK openfda.unii unii YKH834O4BH openfda.unii unii 175F461W10 openfda.unii unii S7V92P67HO openfda.unii unii 4T81LB52R0 openfda.unii unii 9W34L2CQ9A openfda.unii unii 8E272251DI openfda.unii unii 70FD1KFU70 openfda.unii unii 7EA48700V9 openfda.unii unii W8N8R55022 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 care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.