What is NDC 44911-0033?

44911-0033 is the product NDC for Renastat, Saw palmetto 3 [hp_X]/mL + 9 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?

Renastat (Berberis Vulgaris, Petroselinum Sativum, Sabal Serrulata, Uva Ursi, CAntharis, Lithium Carbonicum, Mercurius Corrosivus).

What is the active ingredient?

Saw palmetto, Lytta vesicatoria, Lithium carbonate, Mercuric chloride, Berberis vulgaris root bark, Petroselinum crispum whole, Arctostaphylos uva-ursi leaf, Chondrodendron tomentosum root, Smilax ornata root, Solidago virgaurea flowering top.

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 Renastat?

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.

Renastat NDC 44911-0033 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0033Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0033Add 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
44911-0033-1	4491100330144911003301	30 mL in 1 BOTTLE, DROPPER (44911-0033-1)Marketed from Oct 4, 2012

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): Renastat
Generic name (nonproprietary): berberis vulgaris, petroselinum sativum, sabal serrulata, uva ursi, cantharis, lithium carbonicum, mercurius corrosivus
Active ingredients: Saw palmetto — 3 [hp_X]/mLLytta vesicatoria — 12 [hp_X]/mLLithium carbonate — 12 [hp_X]/mLMercuric chloride — 12 [hp_X]/mLBerberis vulgaris root bark — 3 [hp_X]/mLPetroselinum crispum whole — 3 [hp_X]/mLArctostaphylos uva-ursi leaf — 3 [hp_X]/mLChondrodendron tomentosum root — 12 [hp_X]/mLSmilax ornata root — 12 [hp_X]/mLSolidago virgaurea flowering top — 12 [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 4, 2012
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0033_a3be7ff0-099c-4bed-b83a-80a00725a53cSPL ID a3be7ff0-099c-4bed-b83a-80a00725a53cSPL set ID 78d45c36-271e-40e5-a836-a18a8c580dffUNII J7WWH9M8QS, 3Q034RO3BT, 2BMD2GNA4V, 53GH7MZT1R, 1TH8Q20J0U, 1WZA4Y92EX, 3M5V3D1X36, 395A3P448Z, 2H1576D5WG, 5405K23S50UPC 0363113701739
Pharmacologic class: Mood Stabilizer

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

N444911003301 followed by a unit qualifier and the quantity

Package 44911-0033-01. 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 Oct 30, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve pain in the abdomen extending around to the back, pain in the thighs and loins on urinating and frequent urination.** **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)

About NDC 44911-0033

What is NDC 44911-0033?: 44911-0033 is the product NDC for Renastat, Saw palmetto 3 [hp_X]/mL + 9 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?: Renastat (Berberis Vulgaris, Petroselinum Sativum, Sabal Serrulata, Uva Ursi, CAntharis, Lithium Carbonicum, Mercurius Corrosivus).
What is the active ingredient?: Saw palmetto, Lytta vesicatoria, Lithium carbonate, Mercuric chloride, Berberis vulgaris root bark, Petroselinum crispum whole, Arctostaphylos uva-ursi leaf, Chondrodendron tomentosum root, Smilax ornata root, Solidago virgaurea flowering top.
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 Renastat?: 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.