Hemorrhoids Relief NDC 61727-306

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-306Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0306Add 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
61727-306-21	61727030621	4 g in 1 TUBE (61727-306-21)Marketed from Jul 20, 2012

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): Hemorrhoids Relief
Generic name (nonproprietary): horse chestnut,aloe,hamamelis virginiana root bark/stem bark,nitric acid,paeonia officinalis root,sepia officinalis juice.
Active ingredients: Horse chestnut — 8 [hp_X]/4gAloe — 8 [hp_X]/4gHamamelis virginiana root bark/stem bark — 8 [hp_X]/4gNitric acid — 8 [hp_X]/4gPaeonia officinalis root — 8 [hp_X]/4gSepia officinalis juice — 8 [hp_X]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare Laboratories
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 20, 2012
Listing expires: Dec 31, 2027
Identifiers: Product ID 61727-306_48729b1f-a962-38f5-e063-6394a90a6c18SPL ID 48729b1f-a962-38f5-e063-6394a90a6c18SPL set ID 0e9a1e8b-129f-496c-859b-d71332bd4918UNII 3C18L6RJAZ, V5VD430YW9, T7S323PKJS, 411VRN1TV4, 8R564U2E1P, QDL83WN8C2UPC 0361727306210

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

NDC on a medical claim

N461727030621 followed by a unit qualifier and the quantity

Package 61727-0306-21. 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 Jan 15, 2026.

Indications (excerpt from the label)

Indications & Usage: Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)