Bladder Irritation and UTI NDC 61727-353

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-353Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0353Add 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
61727-353-60	61727035360	60 TABLET, CHEWABLE in 1 BOTTLE (61727-353-60)Marketed from Mar 19, 2019

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): Bladder Irritation and UTI
Generic name (nonproprietary): cantharis, clematis, cubeba, echinacea, ranunculus bulbosus, sabal ser, staphysagria, uva ursi
Active ingredients: Serenoa repens whole — 6 [hp_X]/601Piper cubeba fruit — 6 [hp_X]/601Clematis recta flowering top — 6 [hp_X]/601Arctostaphylos uva-ursi leaf — 6 [hp_X]/601Delphinium staphisagria seed — 6 [hp_X]/601Echinacea angustifolia — 6 [hp_X]/601Lytta vesicatoria — 6 [hp_X]/601Ranunculus bulbosus — 6 [hp_X]/601
Dosage form: Tablet, Chewable
Route: Oral
Labeler: HomeoCare Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 19, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 61727-353_84796173-945e-c70b-e053-2991aa0a4ee1SPL ID 84796173-945e-c70b-e053-2991aa0a4ee1SPL set ID 84796173-945d-c70b-e053-2991aa0a4ee1UNII 487DXM62F2, Z99L7429MA, 396421SP9F, 3M5V3D1X36, 00543AP1JV, VB06AV5US8, 3Q034RO3BT, AEQ8NXJ0MBUPC 0361727353603

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

N461727035360 followed by a unit qualifier and the quantity

Package 61727-0353-60. 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 Mar 19, 2019.

Indications (excerpt from the label)

Uses* Temporarily relieves burning sensation frequent urge to urinate painful urination inflammation

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)