Bladdertone NDC 44911-0597

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0597Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0597Add 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
44911-0597-1	44911059701	30 mL in 1 BOTTLE, DROPPER (44911-0597-1)Marketed from Dec 21, 2020

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): Bladdertone
Generic name (nonproprietary): sarsaparilla, uva-ursi, arsenicum album, cantharis, pareira brava, pulsatilla, sepia, terebinthina, populus tremuloides
Active ingredients: Smilax ornata root — 3 [hp_X]/mLArctostaphylos uva-ursi leaf — 3 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLLytta vesicatoria — 12 [hp_X]/mLChondrodendron tomentosum root — 12 [hp_X]/mLPulsatilla vulgaris whole — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLTurpentine oil — 12 [hp_X]/mLPopulus tremuloides whole — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 21, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0597_e83af16c-70bb-463e-a238-e1d1b314c4ffSPL ID e83af16c-70bb-463e-a238-e1d1b314c4ffSPL set ID 125d7369-f384-4bc1-a1a3-40e8d6a9ea8cUNII 2H1576D5WG, 3M5V3D1X36, S7V92P67HO, 3Q034RO3BT, 395A3P448Z, I76KB35JEV, QDL83WN8C2, C5H0QJ6V7F, MUN0TBE4PEUPC 0363113700893

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

N444911059701 followed by a unit qualifier and the quantity

Package 44911-0597-01. 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 Jul 22, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve intolerable urging, pressure in the area of the bladder, and having to urinate often.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)