Unda 248 NDC 62106-1164

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1164Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1164Add 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
62106-1164-8	62106116408	1 BOTTLE, GLASS in 1 CARTON (62106-1164-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Jul 4, 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 248
Generic name (nonproprietary): crataegus, magnolia grandiflora, passiflora incarnata, strophanthus gratus
Active ingredients: Strophanthus gratus seed — 4 [hp_X]/20mLCrataegus fruit — 4 [hp_X]/20mLMagnolia grandiflora flower — 4 [hp_X]/20mLPassiflora incarnata flowering top — 4 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 4, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 62106-1164_ed123cdf-4e72-2c64-e053-2995a90a59e3SPL ID ed123cdf-4e72-2c64-e053-2995a90a59e3SPL set ID 5383e4f9-337a-74b5-e054-00144ff88e88UNII S81N5ILG2E, Q21UUL2105, RV23PE6426, CLF5YFS11O

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

N462106116408 followed by a unit qualifier and the quantity

Package 62106-1164-08. 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 overall poor circulation symptoms. 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)