FDA.reportPublic FDA data

QueaseX Anti Nausea Drops

Manufacturer
Feelgood Health | W. Last
Effective date
2010-07-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:02:35

Label at a glance#

ProductQueaseX Anti Nausea Drops
Active ingredientSTRYCHNOS NUX-VOMICA SEED, PULSATILLA PATENS, IPECAC, CHAMOMILE, CARDAMOM
Label structure11 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Relieves nausea, vomiting and cramps

INDICATIONS & USAGE SECTION

Indications: Homeopathic remedy relieves the symptoms of nausea and vomiting.

DOSAGE & ADMINISTRATION SECTION

Dosage: Mix 10-15 drops in ¼ cup of water and sip slowly. Repeat every 20 minutes until symptoms subside.

GENERAL PRECAUTIONS SECTION

Caution: Consult your doctor if symptoms persist or worsen.Keep this and all medications out of reach of children.

OTC - ACTIVE INGREDIENT SECTION

Ingredients: Each dose contains equal parts of Nux vom (6C) (HPUS), Pulsatilla (6C) (HPUS), Ipecac (6C) (HPUS), Chamomilla (12C) (HPUS), Zingiber (6C) (HPUS)

INACTIVE INGREDIENT SECTION

Citricidal extract (inactive ingredient).

PREGNANCY SECTION

If pregnant or breastfeeding, ask a health professional before use.

WARNINGS SECTION

Contains no animal products, gluten, artificial flavors, preservatives or colorants. Suitable for vegetarians and safe for all ages.

INFORMATION FOR PATIENTS SECTION

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com

Distributed by

Native Remedies, LLC

6531 Park of Commerce Blvd.

Suite 160

Boca Raton, FL 33487

Phone: 1.877.289.1235

International: + 1.561.999.8857

The letters HPUS indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopoeia of the United States.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottle label
bottle label

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of reach of children.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68647-196-102019-10-21C16284748780-1956f9ecf-d03e-621f-e053-dbdaa90a74adQUEASEX ANTI NAUSEA DROPS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68647-196-10QueaseX Anti Nausea Drops50000 mL in 1 BOTTLE, GLASSTINCTURE500004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68647-196QUEASEX ANTI NAUSEA DROPS (NUX VOM, PULSATILLA , IPECAC, CHAMOMILLA, ZINGIBER) TINCTURE [FEELGOOD HEALTH]4Legacy NDC, 1 package rows20100915_5c24941b-3992-4a52-8c98-48239093c5b5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CARDAMOMACTIVE INGREDIENT8BC4CUT4JL4
CHAMOMILEACTIVE INGREDIENTFGL3685T2X4
IPECACACTIVE INGREDIENT62I3C8233L4
PULSATILLA PATENSACTIVE INGREDIENT4M1169RWJD4
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139194
CARDAMOMACTIVE MOIETY8BC4CUT4JL4
CHAMOMILEACTIVE MOIETYFGL3685T2X4
IPECACACTIVE MOIETY62I3C8233L4
PULSATILLA PATENSACTIVE MOIETY4M1169RWJD4
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139194
CITRUS PARADISI SEEDINACTIVE INGREDIENT12F08874Y74
WATERINACTIVE INGREDIENT059QF0KO0R4

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68647-19668647-196-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PULSATILLA PATENS4M1169RWJDACTIB
IPECAC62I3C8233LACTIB
CHAMOMILEFGL3685T2XACTIB
CARDAMOM8BC4CUT4JLACTIB
CITRUS PARADISI SEED12F08874Y7IACT
WATER059QF0KO0RIACT

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
e8601657-633a-4e7e-9e82-2e6c347c24435c24941b-3992-4a52-8c98-48239093c5b52010-07-17WarningsExact identifier
spl id: e8601657-633a-4e7e-9e82-2e6c347c2443
spl set id: 5c24941b-3992-4a52-8c98-48239093c5b5

Reported adverse events (FAERS/openFDA)#

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