Unda 18 NDC 62106-1117

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1117Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1117Add 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
62106-1117-8	62106111708	1 BOTTLE, GLASS in 1 CARTON (62106-1117-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Feb 6, 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 18
Generic name (nonproprietary): condurango, lycopodium clavatum, viburnum prunifolium, thuja occidentalis, camphora, cuprum metallicum, aluminium metallicum, stibium metallicum
Active ingredients: Antimony — 12 [hp_X]/20mLMarsdenia condurango bark — 5 [hp_X]/20mLViburnum prunifolium bark — 5 [hp_X]/20mLThuja occidentalis leafy twig — 5 [hp_X]/20mLCinnamomum camphora whole — 9 [hp_X]/20mLCopper — 12 [hp_X]/20mLLycopodium clavatum spore — 5 [hp_X]/20mLAluminum — 12 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 6, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 62106-1117_ed104a9f-7380-4f7b-e053-2995a90af948SPL ID ed104a9f-7380-4f7b-e053-2995a90af948SPL set ID 0e71305f-4b5a-6d5a-e054-00144ff88e88UNII 9IT35J3UV3, J411UTU0HN, 1NT28V9397, 0B27814T7X, 789U1901C5, C88X29Y479, CPD4NFA903
Pharmacologic class: Copper-containing Intrauterine Device

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

N462106111708 followed by a unit qualifier and the quantity

Package 62106-1117-08. 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 symptoms associated with low energy tiredness overall exhaustion 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)