Angiplex NDC 62106-1229

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1229Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1229Add 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
62106-1229-3	62106122903	1 BLISTER PACK in 1 BOX (62106-1229-3) / 30 TABLET in 1 BLISTER PACKMarketed from Jan 19, 2015

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): Angiplex
Generic name (nonproprietary): arum triphyllum, aconitum napellus, apis mellifica, belladonna, phytolacca decandra, kali bichromicum, lachesis mutus, mercurius solubilis
Active ingredients: Arisaema triphyllum root — 4 [hp_X]/1Aconitum napellus — 8 [hp_X]/1Apis mellifera — 8 [hp_X]/1Atropa belladonna — 8 [hp_X]/1Phytolacca americana root — 8 [hp_X]/1Potassium dichromate — 10 [hp_X]/1Lachesis muta venom — 10 [hp_X]/1Mercurius solubilis — 10 [hp_X]/1
Dosage form: Tablet
Route: Sublingual
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 19, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 62106-1229_ed11e5b0-cdb3-1f9a-e053-2995a90a0f16SPL ID ed11e5b0-cdb3-1f9a-e053-2995a90a0f16SPL set ID 0d04b1a0-6c43-5f25-e054-00144ff8d46cUNII DM64K844DM, U0NQ8555JD, 7S82P3R43Z, WQZ3G9PF0H, 11E6VI8VEG, T4423S18FM, VSW71SS07I, 324Y4038G2
Pharmacologic class: Standardized Insect Venom Allergenic Extract

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462106122903 followed by a unit qualifier and the quantity

Package 62106-1229-03. 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 9, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with sore throat dry throat Directions Adults and adolescents (12 years and older): At the first sign of symptoms, dissolve one tablet under the tongue every half hour to one hour. When symptoms subside, decrease frequency to every four hours. Once the symptoms are gone, continue taking one tablet daily for three more days. Children (under 12 years): Take under the direction of your healthcare practitioner.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)