What is NDC 44911-0288?

44911-0288 is the product NDC for Prostex HP, Barium carbonate 30 [hp_X]/mL + 10 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Prostex HP (Baryta Carbonica, Clematis Erecta, Conium Maculatum, Lycopodium Clavatum, Mercurius Corrosivus, Pulsatilla (Pratensis), Sabal Serrulata, Selenium Metallicum, Sepia, Staphysagria, Thuja Occidentalis).

What is the active ingredient?

Barium carbonate, Clematis recta flowering top, Conium maculatum flowering top, Lycopodium clavatum spore, Mercuric chloride, Pulsatilla pratensis whole, Saw palmetto, Selenium, Sepia officinalis juice, Delphinium staphisagria seed, Thuja occidentalis leafy twig.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Prostex HP?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Prostex HP NDC 44911-0288 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0288Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0288Add 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
44911-0288-1	4491102880144911028801	30 mL in 1 BOTTLE, DROPPER (44911-0288-1)Marketed from Oct 28, 2015

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): Prostex HPSuffix: HP
Generic name (nonproprietary): baryta carbonica, clematis erecta, conium maculatum, lycopodium clavatum, mercurius corrosivus, pulsatilla (pratensis), sabal serrulata, selenium metallicum, sepia, staphysagria, thuja occidentalis
Active ingredients: Barium carbonate — 30 [hp_X]/mLClematis 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 pratensis 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: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 28, 2015
Listing expires: Dec 31, 2027
Identifiers: Product ID 44911-0288_d51aaf32-6f62-454c-9aa4-e79bcdb18b57SPL ID d51aaf32-6f62-454c-9aa4-e79bcdb18b57SPL set ID 56138252-bc94-41a7-815f-66bab5673a37UNII 6P669D8HQ8, 396421SP9F, Q28R5GF371, C88X29Y479, 53GH7MZT1R, 8E272251DI, J7WWH9M8QS, H6241UJ22B, QDL83WN8C2, 00543AP1JV, 1NT28V9397UPC 0363113701548

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

N444911028801 followed by a unit qualifier and the quantity

Package 44911-0288-01. 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 Aug 26, 2026.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms such as difficult urination, frequent urination at night, and dribbling of urine.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Individual responses may vary, and this product may not work for everyone.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 44911-0288

What is NDC 44911-0288?: 44911-0288 is the product NDC for Prostex HP, Barium carbonate 30 [hp_X]/mL + 10 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Prostex HP (Baryta Carbonica, Clematis Erecta, Conium Maculatum, Lycopodium Clavatum, Mercurius Corrosivus, Pulsatilla (Pratensis), Sabal Serrulata, Selenium Metallicum, Sepia, Staphysagria, Thuja Occidentalis).
What is the active ingredient?: Barium carbonate, Clematis recta flowering top, Conium maculatum flowering top, Lycopodium clavatum spore, Mercuric chloride, Pulsatilla pratensis whole, Saw palmetto, Selenium, Sepia officinalis juice, Delphinium staphisagria seed, Thuja occidentalis leafy twig.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Prostex HP?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.