Pest and Dustmite Formula

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: Pest and Dustmite Formula
Generic name: AMYL NITROSUM, EUPHRASIA OFFICINALIS, KALI MURIATICUM, WYETHIA HELENOIDES, HISTAMINUM HYDROCHLORICUM, LAC CANINUM, GLANDULA SUPRARENALIS SUIS, MUCOSA NASALIS SUIS, ALLIUM CEPA, ARSENICUM ALBUM, BLATTA AMERICANA, IRIDIUM METALLICUM, SABADILLA, SELENIUM METALLICUM, LAC FELINUM, HYALURONIDASE, INTERFERON (SUIS), SEROTONIN (HYDROCHLORIDE), HOUSE DUST MITE
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b1d685d3-a51e-4070-957d-efce7cf91655
SPL ID: 8f13634a-254c-41af-9ad3-64a0a611dcf3
Version: 4
Effective date: 2024-09-27
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:12:43

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Pest and Dustmite Formula	openfda.brand_name
generic name		AMYL NITROSUM, EUPHRASIA OFFICINALIS, KALI MURIATICUM, WYETHIA HELENOIDES, HISTAMINUM HYDROCHLORICUM, LAC CANINUM, GLANDULA SUPRARENALIS SUIS, MUCOSA NASALIS SUIS, ALLIUM CEPA, ARSENICUM ALBUM, BLATTA AMERICANA, IRIDIUM METALLICUM, SABADILLA, SELENIUM METALLICUM, LAC FELINUM, HYALURONIDASE, INTERFERON (SUIS), SEROTONIN (HYDROCHLORIDE), HOUSE DUST MITE	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1548-1	openfda.package_ndc
ndc	product	43742-1548	openfda.product_ndc
ndc11	package	43742154801	derived:openfda.package_ndc
spl id		8f13634a-254c-41af-9ad3-64a0a611dcf3	id
spl set id		b1d685d3-a51e-4070-957d-efce7cf91655	set_id
unii		C9642I91WL	openfda.unii
unii		GKN429M9VS	openfda.unii
unii		3POA0Q644U	openfda.unii
unii		G39P120JQT	openfda.unii
unii		ID3Z1X61WY	openfda.unii
unii		5A3Y60049Z	openfda.unii
unii		44448S9773	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		J10PD1AQ0N	openfda.unii
unii		660YQ98I10	openfda.unii
unii		6NAF1689IO	openfda.unii
unii		492225Q21H	openfda.unii
unii		2RQ1L9N089	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		69404B0LO7	openfda.unii
unii		22T8Z09XAK	openfda.unii
unii		8KOG53Z5EM	openfda.unii
unii		H6241UJ22B	openfda.unii
unii		PR9U2YPF3Q	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: Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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