Hemorrhoidex NDC 34666-405

NDC codes

FDA NDC Directory

Product NDC (as listed)34666-405Labeler and product segments. Claims need a package NDC.

Product NDC at billing width34666-0405Add 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
34666-405-01	34666040501	1 TUBE in 1 CARTON (34666-405-01) / 64.9 g in 1 TUBEMarketed from Dec 30, 2021

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Hemorrhoidex
Generic name (nonproprietary): hamamelis virginiana, ratanhia
Active ingredients: Hamamelis virginiana root bark/stem bark — 1 [hp_X]/64.9gKrameria lappacea root — 3 [hp_X]/64.9g
Dosage form: Gel
Route: Topical
Labeler: Nartex Laboratorios Homeopaticos, S.A. de C.V.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 30, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 34666-405_330fb851-0818-55c2-e063-6294a90ab966SPL ID 330fb851-0818-55c2-e063-6294a90ab966SPL set ID d469349c-1163-1b5d-e053-2a95a90ae83aUNII T7S323PKJS, P29ZH1A35ZUPC 0844827001440

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N434666040501 followed by a unit qualifier and the quantity

Package 34666-0405-01. 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 Apr 18, 2025.

Indications (excerpt from the label)

Uses Temporary soothing and cooling relief of external hemorrhoid symptoms such as itching, burning and relieves external discomfort. Temporary relief of shrinks, swollen, hemorrhoidal tissue. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by FDA, and product has not been clincially tested.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)