FDA.reportPublic FDA data

Nausia

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2022-11-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:48:18

Label at a glance#

ProductNausia
Active ingredientGINGER, IPECAC, IRIS VERSICOLOR ROOT, SKIM MILK, LACTIC ACID, DL-, CYCLAMEN PURPURASCENS TUBER, KEROSENE, TOBACCO LEAF, ARSENIC TRIOXIDE, BRYONIA ALBA ROOT, CADMIUM SULFIDE, ANAMIRTA COCCULUS SEED, COLCHICUM AUTUMNALE BULB, CONIUM MACULATUM FLOWERING TOP, IRON, STRYCHNOS NUX-VOMICA SEED, ANEMONE PRATENSIS, SEPIA OFFICINALIS JUICE, THERIDION CURASSAVICUM, EUPHORBIA COROLLATA ROOT
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Zingiber Officinale 3X, Ipecacuanha 6X, Iris Versicolor 6X, Lac Defloratum 6X, Lacticum Acidum 6X, Cyclamen Europaeum 8X, Petroleum 8X, Tabacum 8X, Arsenicum Album 12X, Bryonia (Alba) 12X, Cadmium Sulphuratum 12X, Cocculus Indicus 12X, Colchicum Autumnale 12X, Conium Maculatum 12X, Ferrum Metallicum 12X, Nux Vomica 12X, Pulsatilla (Pratensis) 12X, Sepia 12X, Theridion 12X, Euphorbia Corollata 24X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of the symptoms of nausea and vomiting associated with pain, pregnancy, vertigo, and headache.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.
If pregnant or breast-feeding, seek advice of a health professional before use.
Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of the symptoms of nausea and vomiting associated with pain, pregnancy, vertigo, and headache.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO
NDC 43742-1314-1
HOMEOPATHIC
NAUSIA
1 FL OZ (30 ml)

NausiaNausia

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-131443742-1314-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
GINGERC5529G5JPQACTIB
IPECAC62I3C8233LACTIB
IRIS VERSICOLOR ROOTX43D4L3DQCACTIB
SKIM MILK6A001Y4M5AACTIB
LACTIC ACID, DL-3B8D35Y7S4ACTIB
CYCLAMEN PURPURASCENS TUBERG728143D8QACTIB
KEROSENE1C89KKC04EACTIB
TOBACCO LEAF6YR2608RSUACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
CADMIUM SULFIDE057EZR4Z7QACTIB
ANAMIRTA COCCULUS SEED810258W28UACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
CONIUM MACULATUM FLOWERING TOPQ28R5GF371ACTIB
IRONE1UOL152H7ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
ANEMONE PRATENSIS8E272251DIACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
THERIDION CURASSAVICUM9Z8D3HEM8LACTIB
EUPHORBIA COROLLATA ROOTZ1UW424Q9ZACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
be2f5366-0c20-4c01-8682-80038f7152f43727a791-bb19-4cdf-999e-64eefa52849e2022-11-11WarningsExact identifier
spl id: be2f5366-0c20-4c01-8682-80038f7152f4
spl set id: 3727a791-bb19-4cdf-999e-64eefa52849e

Reported adverse events (FAERS/openFDA)#

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