FDA.reportPublic FDA data

AngerSoothe

Manufacturer
Feelgood Health | W Last
Effective date
2010-06-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:02:18

Label at a glance#

ProductAngerSoothe
Active ingredientSTRYCHNOS NUX-VOMICA SEED, CHAMOMILE, LYCOPODIUM CLAVATUM SPORE, MINT
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Indications:Homeopathic remedy soothes feelings of anger and prevents temper outbursts.

DOSAGE & ADMINISTRATION SECTION

Dosage:Mix 10 drops in ¼ cup water and sip slowly. Repeat 3-5 times daily as needed until symptoms subside. If preferred, drops may be taken directly into the mouth

GENERAL PRECAUTIONS SECTION

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

DESCRIPTION SECTION


Reduces angry feelings and emotional outbursts.

OTC - ACTIVE INGREDIENT SECTION

Ingredients:Each dose contains equal parts of Nux vom (6C)(HPUS), Chamomilla (6C)(HPUS), Lycopodium (6C)(HPUS).

INACTIVE INGREDIENT SECTION

Peppermint and Citricidal Extract (inactive ingredient).

PREGNANCY SECTION

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

USER SAFETY WARNINGS SECTION

Contains no animal products, gluten, artificial flavors, preservatives, colorants or alcohol. 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 labelBottle label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68647-178-102019-10-21C16284748780-1956f9ecf-de0f-621f-e053-dbdaa90a74adANGERSOOTHE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68647-178-10AngerSoothe50000 mg in 1 BOTTLE, GLASSTINCTURE500002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68647-178ANGERSOOTHE TINCTURE [FEELGOOD HEALTH]2Legacy NDC, 1 package rows20100617_8739d4fe-1353-4cbb-90bf-d804d765a42e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CHAMOMILEACTIVE INGREDIENTFGL3685T2X2
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4792
MINTACTIVE INGREDIENTFV98Z8GITP2
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139192
CHAMOMILEACTIVE MOIETYFGL3685T2X2
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4792
MINTACTIVE MOIETYFV98Z8GITP2
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139192
GRAPEFRUIT SEEDINACTIVE INGREDIENT12F08874Y72
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68647-17868647-178-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
CHAMOMILEFGL3685T2XACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
MINTFV98Z8GITPACTIB
GRAPEFRUIT 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
2102cd03-fdba-4eb3-9dcc-b65ff595c0e18739d4fe-1353-4cbb-90bf-d804d765a42e2010-06-15Exact identifier
spl id: 2102cd03-fdba-4eb3-9dcc-b65ff595c0e1
spl set id: 8739d4fe-1353-4cbb-90bf-d804d765a42e

Reported adverse events (FAERS/openFDA)#

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