Unda 16 NDC 62106-1115

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1115Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1115Add 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
62106-1115-8	62106111508	1 BOTTLE, GLASS in 1 CARTON (62106-1115-8) / 20 mL in 1 BOTTLE, GLASSMarketed from May 7, 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 16
Generic name (nonproprietary): saxifraga granulata, origanum vulgare, lactuca virosa, veronica officinalis, ajuga reptans, drosera, senega officinalis, aurum metallicum, argentum metallicum
Active ingredients: Veronica officinalis flowering top — 4 [hp_X]/20mLAjuga reptans whole — 4 [hp_X]/20mLDrosera rotundifolia flowering top — 4 [hp_X]/20mLPolygala senega root — 4 [hp_X]/20mLGold — 12 [hp_X]/20mLSaxifraga granulata whole — 4 [hp_X]/20mLOriganum vulgare subsp. Hirtum whole — 4 [hp_X]/20mLLactuca virosa — 4 [hp_X]/20mLSilver — 12 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 7, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 62106-1115_c731175a-04a5-5d25-e053-2995a90a6082SPL ID c731175a-04a5-5d25-e053-2995a90a6082SPL set ID 1583cf73-c22c-0fa8-e054-00144ff8d46cUNII 9Q24RAI43V, 3M4G523W1G, 74068FOS7R, G0R4UBI2ZZ, W1LUS9R48G, KPS1B1162N, 2FXJ6SW4PK, M7T6H7D4IF, 6D74QW4H67, 79Y1949PYO, S7V92P67HO, 9IH82J936J, 1NT28V9397, 38SNL0F81Z, CPD4NFA903, 387GMG9FH5, 3M5V3D1X36, XZC6H8R666, 1DP6Y6B65Z, 18E7415PXQ, C88X29Y479, E678D1QH0K, 75O014T1HG, 0R715588D2, 464910T5N9, 2P299V784P, Q4EWM09M3OUPC 0883196301102
Pharmacologic class: Standardized Chemical Allergen

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

N462106111508 followed by a unit qualifier and the quantity

Package 62106-1115-08. 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 Jul 15, 2021.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with abdominal cramping, bloating and gas following meals. 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)