Spectric NDC 43742-1177

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1177Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1177Add 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
43742-1177-1	43742117701	30 mL in 1 BOTTLE, DROPPER (43742-1177-1)Marketed from Feb 20, 2018

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Spectric
Generic name (nonproprietary): ethylicum, kali bromatum, aspartic acid, l-dopa, serotonin (hydrochloride), cerebrum suis, placenta totalis suis, agaricus muscarius, bufo rana, helleborus niger, hyoscyamus niger, olibanum (boswellia serrata), stramonium, thuja occidentalis, helium, neon, carcinosin, hydrogen
Active ingredients: Alcohol — 6 [hp_X]/mLPotassium bromide — 6 [hp_X]/mLAspartic acid — 6 [hp_X]/mLLevodopa — 6 [hp_X]/mLSerotonin hydrochloride — 6 [hp_X]/mLSus scrofa cerebrum — 8 [hp_X]/mLSus scrofa placenta — 8 [hp_X]/mLAmanita muscaria fruiting body — 12 [hp_X]/mLBufo bufo cutaneous gland — 12 [hp_X]/mLHelleborus niger root — 12 [hp_X]/mLHyoscyamus niger — 12 [hp_X]/mLIndian frankincense — 12 [hp_X]/mLDatura stramonium — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLHelium — 16 [hp_X]/mLNeon — 16 [hp_X]/mLHuman breast tumor cell — 30 [hp_X]/mLHydrogen — 12 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 20, 2018
Marketing end: Jul 1, 2027
Other FDA classes: Aromatic (Chemical structure)
Identifiers: Product ID 43742-1177_d1c4ceb6-8627-496e-b632-402fe68c2d49SPL ID d1c4ceb6-8627-496e-b632-402fe68c2d49SPL set ID 3e534017-4a9f-42a2-bdfd-1e8c73c0515aUNII 3K9958V90M, OSD78555ZM, 30KYC7MIAI, 46627O600J, GKN429M9VS, 4GB5DQR532, C8CV8867O8, DIF093I037, Q59QU6N72Q, 608DGJ6815, 4WRK2153H3, 4PW41QCO2M, G6W4F0V8Z3, 1NT28V9397, 206GF3GB41, 4VB4Y46AHD, C62OO7VD9K, 7YNJ3PO35Z
Pharmacologic class: Aromatic Amino Acid

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

N443742117701 followed by a unit qualifier and the quantity

Package 43742-1177-01. 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 Nov 8, 2022.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms such as agitation, lack of empathy, angry outburst, repetitive behaviors, repetitive speech, delayed language development, indifferent to human interaction, and precocity.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)