Unda 219 NDC 62106-1156

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1156Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1156Add 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
62106-1156-8	62106115608	1 BOTTLE, GLASS in 1 CARTON (62106-1156-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Mar 27, 2016

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 219
Generic name (nonproprietary): crataegus, lactuca virosa, passiflora incarnata, thymus vulgaris, valeriana officinalis
Active ingredients: Lactuca virosa — 4 [hp_X]/20mLCrataegus fruit — 4 [hp_X]/20mLThyme — 4 [hp_X]/20mLPassiflora incarnata flowering top — 4 [hp_X]/20mLValerian — 4 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 27, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 62106-1156_ed10cda7-03ea-2f5e-e053-2a95a90a0500SPL ID ed10cda7-03ea-2f5e-e053-2a95a90a0500SPL set ID 2f0cd4d0-55ab-64b4-e054-00144ff8d46cUNII 6D74QW4H67, Q21UUL2105, CW657OBU4N, CLF5YFS11O, JWF5YAW3QWUPC 0883196302208
Pharmacologic class: Non-Standardized Food 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462106115608 followed by a unit qualifier and the quantity

Package 62106-1156-08. 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 Helps to promote relaxation and temporarily relieve mild nervousness 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)