What is NDC 44911-0323?

44911-0323 is the product NDC for Intestipar, Gentiana lutea root 3 [hp_X]/mL + 6 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?

Intestipar (Gentiana Lutea, Arsenicum Album, Cinchona Officinalis, Colocynthis, Nux Vomica, Phosphorus, Small Intestine (Suis)).

What is the active ingredient?

Gentiana lutea root, Arsenic trioxide, Cinchona officinalis bark, Citrullus colocynthis fruit pulp, Strychnos nux-vomica seed, Phosphorus, Pork intestine.

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 Intestipar?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Intestipar NDC 44911-0323 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0323Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0323Add 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
44911-0323-1	4491103230144911032301	30 mL in 1 BOTTLE, DROPPER (44911-0323-1)Marketed from Feb 12, 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): Intestipar
Generic name (nonproprietary): gentiana lutea, arsenicum album, cinchona officinalis, colocynthis, nux vomica, phosphorus, small intestine (suis)
Active ingredients: Gentiana lutea root — 3 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLCinchona officinalis bark — 12 [hp_X]/mLCitrullus colocynthis fruit pulp — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPork intestine — 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: Feb 12, 2016
Marketing end: Feb 6, 2029
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0323_ce190053-2de1-4275-8276-bf1dd910384cSPL ID ce190053-2de1-4275-8276-bf1dd910384cSPL set ID 23d5328e-ee8d-48d9-811f-7aa7be59d19eUNII S72O3284MS, S7V92P67HO, S003A158SB, 23H32AOH17, 269XH13919, 27YLU75U4W, 40GMI0R60LUPC 0363113700671
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N444911032301 followed by a unit qualifier and the quantity

Package 44911-0323-01. 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 May 6, 2026.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve weak digestion, bloating, abdominal, pain and diarrhea.** **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 44911-0323

What is NDC 44911-0323?: 44911-0323 is the product NDC for Intestipar, Gentiana lutea root 3 [hp_X]/mL + 6 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?: Intestipar (Gentiana Lutea, Arsenicum Album, Cinchona Officinalis, Colocynthis, Nux Vomica, Phosphorus, Small Intestine (Suis)).
What is the active ingredient?: Gentiana lutea root, Arsenic trioxide, Cinchona officinalis bark, Citrullus colocynthis fruit pulp, Strychnos nux-vomica seed, Phosphorus, Pork intestine.
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 Intestipar?: 1 other product NDC are listed under this name. See all Intestipar NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Intestipar NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Intestipargentiana lutea, arsenicum album, berberinum, cinchona officinalis, colocynthis, hydrastis canadensis, indolum, lycopodium clavatum, natrum sulphuricum, nux vomica, phosphorus, small intestine (suis)	Gentiana lutea root 3 [hp_X]/mL + 11 more ingredients	LiquidOral	Energique, Inc.	44911-0908	44911-0908-01