NativeRemedies BrightSpark Oral Spray

Manufacturer
Silver Star Brands | King Bio
Effective date
2016-03-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:26:01

Label at a glance#

ProductBrightSpark
Active ingredientSILVER NITRATE, VERATRUM ALBUM ROOT, ARSENIC TRIIODIDE, HYOSCYAMUS NIGER
Label structure10 sections

Indications and uses

Homeopathic remedy for distractability, mood and restlessness; assists with concentration. *This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Dosage and administration

Initially depress pump until primed. Hold close to mouth and spray directly into mouth. Use three times daily. Use additionally as needed. Adults: 3 pump sprays. Children 2-12: 2 pump sprays.

Label contents#

Full prescribing information#

HPUS Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Each dose contains equal parts of: Arg nit 6C, Arsenicum iod 30C, Hyoscyamus 30C, Veratrum alb 30C.

Uses

INDICATIONS & USAGE SECTION

Homeopathic remedy for distractability, mood and restlessness; assists with concentration.

*This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Warnings

WARNINGS SECTION

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

Initially depress pump until primed. Hold close to mouth and spray directly into mouth. Use three times daily. Use additionally as needed. Adults: 3 pump sprays. Children 2-12: 2 pump sprays.

Other Information

OTHER SAFETY INFORMATION

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

Contains no artificial flavors or artificial colors. No gluten added.

INACTIVE INGREDIENT SECTION

Citric acid, potassium sorbate, purified water.

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 Control Center right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - PURPOSE SECTION

Relieves hyperactivity, distractibility & impulsiveness

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BrightSpark Oral SprayBrightSpark Oral Spray

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68703-252-022020-02-11C16284748780-19d75b9d0-5ecf-f424-e053-dadaa90a57ceNativeRemedies BrightSpark Oral Spray
68703-252-022020-01-31C16284748780-19d75b9d0-5ecf-f424-e053-dadaa90a57ceNativeRemedies BrightSpark Oral Spray

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68703-25268703-252-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
286894e1-f6f8-1f1d-e063-6394a90aef892eb93d7c-330f-4b93-e054-00144ff88e882024-12-03WarningsExact identifier
spl set id: 2eb93d7c-330f-4b93-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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