Nausia

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: Nausia
Generic name: ARSENICUM ALBUM, BRYONIA (ALBA), CADMIUM SULPHURATUM, COCCULUS INDICUS, COLCHICUM AUTUMNALE, CONIUM MACULATUM, CYCLAMEN EUROPAEUM, EUPHORBIA COROLLATA, FERRUM METALLICUM, IPECACUANHA, IRIS VERSICOLOR, LAC DEFLORATUM, LACTICUM ACIDUM, NUX VOMICA, PETROLEUM, PULSATILLA (PRATENSIS), SEPIA, TABACUM, THERIDION, ZINGIBER OFFICINALE
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 025ed334-29dd-4519-b9f6-cf560e73c294
SPL ID: d81047b4-324b-4afa-bf9d-f9553cbf9f08
Version: 1
Effective date: 2024-09-23
Source export date: 2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:28:35

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		Nausia	openfda.brand_name
generic name		ARSENICUM ALBUM, BRYONIA (ALBA), CADMIUM SULPHURATUM, COCCULUS INDICUS, COLCHICUM AUTUMNALE, CONIUM MACULATUM, CYCLAMEN EUROPAEUM, EUPHORBIA COROLLATA, FERRUM METALLICUM, IPECACUANHA, IRIS VERSICOLOR, LAC DEFLORATUM, LACTICUM ACIDUM, NUX VOMICA, PETROLEUM, PULSATILLA (PRATENSIS), SEPIA, TABACUM, THERIDION, ZINGIBER OFFICINALE	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-2198-1	openfda.package_ndc
ndc	product	43742-2198	openfda.product_ndc
ndc11	package	43742219801	derived:openfda.package_ndc
spl id		d81047b4-324b-4afa-bf9d-f9553cbf9f08	id
spl set id		025ed334-29dd-4519-b9f6-cf560e73c294	set_id
unii		269XH13919	openfda.unii
unii		993QHL78E6	openfda.unii
unii		6A001Y4M5A	openfda.unii
unii		057EZR4Z7Q	openfda.unii
unii		G728143D8Q	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		Z1UW424Q9Z	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		6YR2608RSU	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		3B8D35Y7S4	openfda.unii
unii		8E272251DI	openfda.unii
unii		62I3C8233L	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		E1UOL152H7	openfda.unii
unii		810258W28U	openfda.unii
unii		9Z8D3HEM8L	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		C5529G5JPQ	openfda.unii
unii		1C89KKC04E	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.