Unda 39 NDC 62106-1138

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1138Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1138Add 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
62106-1138-8	62106113808	1 BOTTLE, GLASS in 1 CARTON (62106-1138-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Jan 16, 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 39
Generic name (nonproprietary): asafoetida gum resin,absinthium, allium cepa, tanacetum vulgare aerial parts, cina flower-heads, dryopteris filix-mas rhizome, argentum metallicum
Active ingredients: Dryopteris filix-mas root — 6 [hp_X]/20mLArtemisia cina pre-flowering top — 6 [hp_X]/20mLSilver — 12 [hp_X]/20mLAsafetida — 4 [hp_X]/20mLWormwood — 4 [hp_X]/20mLOnion — 4 [hp_X]/20mLTanacetum vulgare 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: Jan 16, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 62106-1138_ebe17695-25c1-19f2-e053-2a95a90a66baSPL ID ebe17695-25c1-19f2-e053-2a95a90a66baSPL set ID 0cc8aa90-b341-1f90-e054-00144ff88e88UNII C0ZK0RRF5X, 28M1820ACT, 3M4G523W1G, W9FZA51AS1, F84709P2XV, 492225Q21H, D52957JQ8M
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

N462106113808 followed by a unit qualifier and the quantity

Package 62106-1138-08. 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 Oct 25, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of minor symptoms associated with irritability and anxiousness. 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)