Brightspark NDC 68703-358

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-358Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0358Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
68703-358-80	68703035880	180 TABLET in 1 BOTTLE, GLASS (68703-358-80)Marketed from Dec 25, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Brightspark
Generic name (nonproprietary): arg nit, arsenicum iod, hyoscyamus, veratrum alb
Active ingredients: Silver nitrate — 6 [hp_C]/1801Veratrum album root — 30 [hp_C]/1801Arsenic triiodide — 30 [hp_C]/1801Hyoscyamus niger leaf — 30 [hp_C]/1801
Dosage form: Tablet
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 25, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 68703-358_2ab10b12-68ed-3af8-e063-6294a90af21fSPL ID 2ab10b12-68ed-3af8-e063-6294a90af21fSPL set ID b6c50a09-7c13-e1c5-e053-2a95a90a0610UNII 95IT3W8JZE, QNS6W5US1Z, 3029988O2T, 32IT7G8BAWUPC 0810845010306

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468703035880 followed by a unit qualifier and the quantity

Package 68703-0358-80. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 1, 2025.

Indications (excerpt from the label)

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.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)