NDC 68703-358 Brightspark

Arg Nit, Arsenicum Iod, Hyoscyamus, Veratrum Alb

NDC Product Information

Brightspark with NDC 68703-358 is a a human over the counter drug product labeled by Silver Star Brands. The generic name of Brightspark is arg nit, arsenicum iod, hyoscyamus, veratrum alb. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Silver Star Brands

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Brightspark Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SILVER NITRATE 6 [hp_C]/1801
  • VERATRUM ALBUM ROOT 30 [hp_C]/1801
  • ARSENIC TRIIODIDE 30 [hp_C]/1801
  • HYOSCYAMUS NIGER LEAF 30 [hp_C]/1801

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • SUCROSE (UNII: C151H8M554)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Silver Star Brands
Labeler Code: 68703
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 12-25-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Brightspark Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Hpus Active Ingredients

HPUS Active Ingredients: Each tablet contains equal parts of: Arg nit 6C, Arsenicum iod 30C, Hyoscyamus 30C, Veratrum alb 30C.

Uses*

Uses*: Homeopathic remedy for distractibility, mood, and restlessness; assists with concentration.*Claims based on traditional homeopathic practice, not accepted medical evidence. Not evaluated by the FDA.

Warnings

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

Directions: Chew or dissolve tablets in the mouth. Alternatively, crush and sprinkle directly on the tongue or mix in warm water or soft food. For all ages: Take 2 tablets 3 times daily on an empty stomach when possible.Initial dose only: Take 1 tablet every hour for 6 hours.

Other Safety Information

Tamper resistant for your proection. Use only if saftey seal is intact.Contains no artificial flavors or colorants. No gluten added. Lactose-free.

Inactive Ingredients

Inactive Ingredients: Magnesium stearat, Maltodextrin, Sucrose.

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children.

Otc - Pregnancy Or Breast Feeding

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

Otc - Purpose

Relieves hyperactivity distractibility & impulsiveness.

* Please review the disclaimer below.