Dizzy

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: Dizzy
Generic name: CEREBELLUM (SUIS), BRYONIA (ALBA), PETROLEUM, TABACUM, AMBRA GRISEA, CYCLAMEN EUROPAEUM, NATRUM SALICYLICUM, ARGENTUM NITRICUM, ASARUM CANADENSE, CALCAREA SULPHURICA, CARBONEUM SULPHURATUM, CHININUM SULPHURICUM, COCCULUS INDICUS, CONIUM MACULATUM, DIGITALIS PURPUREA, GELSEMIUM SEMPERVIRENS, PHOSPHORUS, PIPER METHYSTICUM, SILICEA, THERIDION
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: fdf934f8-7b12-4076-b8fb-00c095940697
SPL ID: 7581a689-8459-41c1-8546-c99d733347ad
Version: 4
Effective date: 2024-03-15
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:46:35

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Dizzy	openfda.brand_name
generic name		CEREBELLUM (SUIS), BRYONIA (ALBA), PETROLEUM, TABACUM, AMBRA GRISEA, CYCLAMEN EUROPAEUM, NATRUM SALICYLICUM, ARGENTUM NITRICUM, ASARUM CANADENSE, CALCAREA SULPHURICA, CARBONEUM SULPHURATUM, CHININUM SULPHURICUM, COCCULUS INDICUS, CONIUM MACULATUM, DIGITALIS PURPUREA, GELSEMIUM SEMPERVIRENS, PHOSPHORUS, PIPER METHYSTICUM, SILICEA, THERIDION	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1675-1	openfda.package_ndc
ndc	product	43742-1675	openfda.product_ndc
ndc11	package	43742167501	derived:openfda.package_ndc
spl id		7581a689-8459-41c1-8546-c99d733347ad	id
spl set id		fdf934f8-7b12-4076-b8fb-00c095940697	set_id
unii		27YLU75U4W	openfda.unii
unii		4GB5DQR532	openfda.unii
unii		E2O4O7TQYK	openfda.unii
unii		E934B3V59H	openfda.unii
unii		BOW48C81XP	openfda.unii
unii		G728143D8Q	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		WIQ1H85SYP	openfda.unii
unii		S54S8B99E8	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		6YR2608RSU	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		XTC0D02P6C	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		810258W28U	openfda.unii
unii		9Z8D3HEM8L	openfda.unii
unii		F1T8QT9U8B	openfda.unii
unii		1C89KKC04E	openfda.unii
unii		KF7Z0E0Q2B	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, contact a physician or Poison Control Center right away. Tamper Evident: 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.