Unda 600 NDC 62106-1170

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1170Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1170Add 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
62106-1170-8	62106117008	1 BOTTLE, GLASS in 1 CARTON (62106-1170-8) / 20 mL in 1 BOTTLE, GLASSMarketed from May 5, 2017

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 600
Generic name (nonproprietary): berberis vulgaris, rheum, rhus toxicodendron
Active ingredients: Rheum officinale root — 6 [hp_X]/20mLBerberis vulgaris root bark — 6 [hp_X]/20mLToxicodendron pubescens shoot — 6 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 5, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 62106-1170_ed12a71d-e8f3-b336-e053-2a95a90a4f09SPL ID ed12a71d-e8f3-b336-e053-2a95a90a4f09SPL set ID 4d505bd6-2819-6c7f-e054-00144ff88e88UNII A47JP5ZG9M, 1TH8Q20J0U, 46PYZ1F82M

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

N462106117008 followed by a unit qualifier and the quantity

Package 62106-1170-08. 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 Nov 9, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of occasional muscle stiffness. 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)