NDC codes

FDA NDC Directory
Product NDC (as listed)62106-1171Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62106-1171Add 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 NDC11-digit (billing)PackageCopy
62106-1171-862106117108621061171081 BOTTLE, GLASS in 1 CARTON (62106-1171-8) / 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 700
Generic name (nonproprietary)
berberis vulgaris, calcarea fluorica
Active ingredients
Berberis vulgaris root bark — 4 [hp_X]/20mLCalcium fluoride — 12 [hp_X]/20mL
Dosage form
Liquid
Route
Oral
Labeler
Seroyal USANDC labeler code 62106
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 62106-1171_c733ec78-5b43-7a7c-e053-2995a90a2f9aSPL ID c733ec78-5b43-7a7c-e053-2995a90a2f9aSPL set ID 206a5750-2025-205e-e054-00144ff8d46cUNII 75O014T1HG, 046Y1357I6, IDB0NAZ6AI, M7T6H7D4IF, 1TH8Q20J0U, O3B55K4YKI, DTN01M69SN, YQ2S06L8S9, Q1RGP4UB73UPC 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

N462106117108 followed by a unit qualifier and the quantity

Package 62106-1171-08. 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 .

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)

About NDC 62106-1171

What is NDC 62106-1171?
62106-1171 is the product NDC for Unda 700, Berberis vulgaris root bark 4 [hp_X]/20mL; Calcium fluoride 12 [hp_X]/20mL liquid, listed with the FDA by Seroyal USA. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Unda 700 (Berberis vulgaris, Calcarea fluorica).
What is the active ingredient?
Berberis vulgaris root bark, Calcium fluoride.
Who is the labeler?
Seroyal USA, NDC labeler code 62106. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Unda 700?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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