Histastat Pollen

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: Histastat Pollen
Generic name: BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), ADRENALINUM, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM ALBUM, EUPHRASIA OFFICINALIS, HISTAMINUM HYDROCHLORICUM, NATRUM MURIATICUM, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), SABADILLA, SINAPIS NIGRA, SOLIDAGO VIRGAUREA, SULPHUR, WYETHIA HELENIOIDES
Manufacturer: Energique, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 00478787-ccec-4101-a0da-fd337037c3ee
SPL ID: cb42e9ee-cc8f-417e-8d39-3e4a72e8204d
Version: 1
Effective date: 2023-05-12
Source export date: 2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:19

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Histastat Pollen	openfda.brand_name
generic name		BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), ADRENALINUM, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM ALBUM, EUPHRASIA OFFICINALIS, HISTAMINUM HYDROCHLORICUM, NATRUM MURIATICUM, NATRUM SULPHURICUM, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), SABADILLA, SINAPIS NIGRA, SOLIDAGO VIRGAUREA, SULPHUR, WYETHIA HELENIOIDES	openfda.generic_name
manufacturer name		Energique, Inc.	openfda.manufacturer_name
ndc	package	44911-0674-1	openfda.package_ndc
ndc	product	44911-0674	openfda.product_ndc
ndc11	package	44911067401	derived:openfda.package_ndc
spl id		cb42e9ee-cc8f-417e-8d39-3e4a72e8204d	id
spl set id		00478787-ccec-4101-a0da-fd337037c3ee	set_id
unii		27YLU75U4W	openfda.unii
unii		C9642I91WL	openfda.unii
unii		269XH13919	openfda.unii
unii		3POA0Q644U	openfda.unii
unii		0YPR65R21J	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		YKH834O4BH	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		J10PD1AQ0N	openfda.unii
unii		9W34L2CQ9A	openfda.unii
unii		8LTY55LQ8D	openfda.unii
unii		6NAF1689IO	openfda.unii
unii		492225Q21H	openfda.unii
unii		8E272251DI	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		5EF0HWI5WU	openfda.unii
unii		5405K23S50	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. 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 a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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