Unda 312 NDC 62106-1169

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1169Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1169Add 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
62106-1169-8	62106116908	1 BOTTLE, GLASS in 1 CARTON (62106-1169-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Sep 23, 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): Unda 312
Generic name (nonproprietary): angelica archangelica, drosera, grindelia, lamium album, pinus sylvestris, rubus fruticosus, senega officinalis
Active ingredients: Drosera rotundifolia flowering top — 6 [hp_X]/20mLGrindelia hirsutula flowering top — 6 [hp_X]/20mLPinus sylvestris leafy twig — 6 [hp_X]/20mLAngelica archangelica root — 6 [hp_X]/20mLLamium album — 6 [hp_X]/20mLRubus fruticosus leaf — 6 [hp_X]/20mLPolygala senega root — 6 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 23, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 62106-1169_c733ec78-5b43-7a7c-e053-2995a90a2f9aSPL ID c733ec78-5b43-7a7c-e053-2995a90a2f9aSPL set ID 206a5750-2025-205e-e054-00144ff8d46cUNII Q1RGP4UB73, 75O014T1HG, 1TH8Q20J0U, M7T6H7D4IF, YQ2S06L8S9, O3B55K4YKI, DTN01M69SN, IDB0NAZ6AI, 046Y1357I6UPC 0883196304608

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

N462106116908 followed by a unit qualifier and the quantity

Package 62106-1169-08. 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 Jul 15, 2021.

Indications (excerpt from the label)

Uses For the relief of symptoms associated with sore throat. Directions Adults and adolescents (12 years and older): Take 5 drops three times daily or as recommended by your healthcare practitioner. 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)