Unda 36 NDC 62106-1135

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1135Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1135Add 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
62106-1135-8	62106113508	1 BOTTLE, GLASS in 1 CARTON (62106-1135-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Dec 14, 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 36
Generic name (nonproprietary): aconitum napellus, aesculus hippocastanum, aluminium metallicum, chelidonium majus, hamamelis virginiana, hydrastis canadensis, hypericum perforatum
Active ingredients: Aconitum napellus — 4 [hp_X]/20mLHorse chestnut — 4 [hp_X]/20mLAluminum — 12 [hp_X]/20mLChelidonium majus root — 4 [hp_X]/20mLHamamelis virginiana bark — 4 [hp_X]/20mLGoldenseal — 4 [hp_X]/20mLHypericum perforatum — 4 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 14, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 62106-1135_ed10a778-ddc9-c29c-e053-2995a90aa5c3SPL ID ed10a778-ddc9-c29c-e053-2995a90aa5c3SPL set ID 26e7d64b-1a94-6de4-e054-00144ff8d46cUNII U0NQ8555JD, 3C18L6RJAZ, CPD4NFA903, FLT36UCF0N, IH3063S9MY, ZW3Z11D0JV, XK4IUX8MNB

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

N462106113508 followed by a unit qualifier and the quantity

Package 62106-1135-08. 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 mild symptoms associated with hemorrhoids. 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)