Uroflo HP NDC 43406-0636

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0636Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0636Add 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
43406-0636-1	43406063601	30 mL in 1 BOTTLE, DROPPER (43406-0636-1)Marketed from Jul 6, 2016

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): Uroflo HP
Generic name (nonproprietary): clematis erecta, conium maculatum, lycopodium clavatum, mercurius corrosivus, pulsatilla, sabal serrulata, selenium metallicum, sepia, staphysagria, thuja occidentalis
Active ingredients: Clematis recta flowering top — 30 [hp_X]/mLConium maculatum flowering top — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLMercuric chloride — 30 [hp_X]/mLPulsatilla vulgaris whole — 30 [hp_X]/mLSaw palmetto — 30 [hp_X]/mLSelenium — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mLDelphinium staphisagria seed — 30 [hp_X]/mLThuja occidentalis leafy twig — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 6, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 43406-0636_ae23e393-9792-495b-8d15-9b36e506ea20SPL ID ae23e393-9792-495b-8d15-9b36e506ea20SPL set ID 7a150bad-e709-46f3-b4c8-f045a30092fbUNII 396421SP9F, Q28R5GF371, C88X29Y479, 53GH7MZT1R, I76KB35JEV, J7WWH9M8QS, H6241UJ22B, QDL83WN8C2, 00543AP1JV, 1NT28V9397UPC 0877730004710

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

N443406063601 followed by a unit qualifier and the quantity

Package 43406-0636-01. 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 Dec 18, 2025.

Indications (excerpt from the label)

USES: Termporarily relieves urinary frequency and urgency.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)