GI Clear P NDC 44911-0611

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0611Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0611Add 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
44911-0611-1	44911061101	60 mL in 1 BOTTLE, DROPPER (44911-0611-1)Marketed from Jun 21, 2021

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): GI Clear P
Generic name (nonproprietary): arsenicum album, baptisia tinctoria, lachesis mutus, pulsatilla (pratensis), rhus tox
Active ingredients: Arsenic trioxide — 10 [hp_X]/mLBaptisia tinctoria root — 10 [hp_X]/mLLachesis muta venom — 10 [hp_X]/mLPulsatilla pratensis whole — 10 [hp_X]/mLToxicodendron pubescens leaf — 10 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 21, 2021
Marketing end: Dec 12, 2028
Identifiers: Product ID 44911-0611_787bc0d6-e847-4983-b9eb-e1bbba4c7c9cSPL ID 787bc0d6-e847-4983-b9eb-e1bbba4c7c9cSPL set ID 9aca850f-7e18-4147-aaf1-f6f04047f7f3UNII S7V92P67HO, 5EF0HWI5WU, VSW71SS07I, 8E272251DI, 6IO182RP7AUPC 0363113701272

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

N444911061101 followed by a unit qualifier and the quantity

Package 44911-0611-01. 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 16, 2025.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve nausea, diarrhea, abdominal cramping, gas, bloatin, dehydration, and fever.** **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)