NativeRemedies Anger-Soothe

Manufacturer
Silver Star Brands | OHM Pharma
Effective date
2025-01-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:30:01

Label at a glance#

ProductNativeRemedies Anger-Soothe
Active ingredientSTRYCHNOS NUX-VOMICA SEED, MATRICARIA RECUTITA, LYCOPODIUM CLAVATUM SPORE
Label structure10 sections

Indications and uses

Uses*: Homeopathic remedy soothes feelings of anger and prevents temper outbursts. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

Directions: For all ages: Mix 0.50 mL in 1/4 cup water and sip slowly. Alternatively, drops may be taken directly into the mouth. Use 3-5 times daily as needed until symptoms improve.

Label contents#

Full prescribing information#

HPUS Active Ingrediients

OTC - ACTIVE INGREDIENT SECTION

HPUS Active Ingredients: Equal volumes of each ingredient in a 6C potency: Chamomilla, Lycopodium, Nux vomica.

The letters HPUS indicate that the components in this product are offically monographed in the Homeopathic Pharmacopoeia of the United States.

Uses*:

INDICATIONS & USAGE SECTION

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

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS SECTION

Warnings: If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a health professional before use. Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: For all ages: Mix 0.50 mL in 1/4 cup water and sip slowly. Alternatively, drops may be taken directly into the mouth. Use 3-5 times daily as needed until symptoms improve.

OTHER SAFETY INFORMATION

Contains no artificial flavors or colorants. No gluten added.

Tamper resistant for your protection. Use only if safety seal is intact.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Purified water, USP grain alcohol (20% by volume).

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Conrtol Center right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - PURPOSE SECTION

Reduces angry feelings & emotional outbursts.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Anger-SootheAnger-Soothe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68703-392-02NativeRemedies Anger-Soothe59 mL in 1 BOTTLE, DROPPERLIQUID593

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68703-392NATIVEREMEDIES ANGER-SOOTHE (CHAMOMILLA, LYCOPODIUM, NUX VOMICA) LIQUID [SILVER STAR BRANDS]3Current NDC, 1 package rows20250103_f67f7955-c4e9-64d7-e053-2995a90ac756.zip

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
68703-39268703-392-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
NativeRemedies Anger-SootheCHAMOMILLA, LYCOPODIUM, NUX VOMICASilver Star Brandsf67f7955-c4e9-64d7-e053-2995a90ac7562025-01-01WarningsExact identifier
ndc (package): 68703-392-02
ndc (product): 68703-392
ndc11 (package): 68703039202
spl id: 2ab0f66a-fdb0-1f10-e063-6294a90af7bc
spl set id: f67f7955-c4e9-64d7-e053-2995a90ac756

Reported adverse events (FAERS/openFDA)#

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