Chemstat NDC 44911-0556

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0556Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0556Add 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
44911-0556-1	44911055601	30 mL in 1 BOTTLE, DROPPER (44911-0556-1)Marketed from Oct 7, 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): Chemstat
Generic name (nonproprietary): glycerinum, taraxacum officinale, phytolacca decandra, arsenicum album, nitricum acidum, nux vomica, petroleum, phosphoricum acidum, phosphorus, acetylsalicylicum acidum, glonoinum, insulinum (human), lithium carbonicum, thyroidinum (suis), aceticum acidum, benzoicum acidum, benzyl alcohol, boricum acidum, chlorinum, cortisone aceticum, eugenol, folliculinum, isopropyl palmitate, lacticum acidum, petroleum jelly, phenyl butazone, plumbum metallicum, potassium sorbate, resorcinum, salicylicum acidum,
Active ingredients: Glycerin — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLKerosene — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLAspirin — 12 [hp_X]/mLNitroglycerin — 12 [hp_X]/mLInsulin human — 12 [hp_X]/mLLithium carbonate — 12 [hp_X]/mLThyroid — 12 [hp_X]/mLAcetic acid — 12 [hp_X]/mLBenzoic acid — 12 [hp_X]/mLBenzyl alcohol — 12 [hp_X]/mLBoric acid — 12 [hp_X]/mLChlorine — 12 [hp_X]/mLCortisone acetate — 12 [hp_X]/mLEugenol — 12 [hp_X]/mLEstrone — 12 [hp_X]/mLIsopropyl palmitate — 12 [hp_X]/mLLactic acid, Dl- — 12 [hp_X]/mLPotassium sorbate — 12 [hp_X]/mLPetrolatum — 12 [hp_X]/mLPhenylbutazone — 12 [hp_X]/mLLead — 12 [hp_X]/mLResorcinol — 12 [hp_X]/mLSalicylic acid — 12 [hp_X]/mLStearyl alcohol — 12 [hp_X]/mLSorbitol — 12 [hp_X]/mLXylitol — 12 [hp_X]/mLCorticotropin — 15 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 7, 2020
Marketing end: Aug 2, 2029
Other FDA classes: Adrenocorticotropic Hormone (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Ammonium Ion Binding Activity (Mechanism)Non-Steroidal (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Corticosteroid Hormone Receptor Agonists (Mechanism)Cyclooxygenase Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)Decreased Prostaglandin Production (Physiologic effect)Glycerol (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Insulin (Chemical structure)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 44911-0556_31037a1d-f6c7-49be-8557-a86ef771a188SPL ID 31037a1d-f6c7-49be-8557-a86ef771a188SPL set ID 2831d28e-9cf1-4a72-9c6c-bb014d059558UNII PDC6A3C0OX, 39981FM375, 11E6VI8VEG, S7V92P67HO, 411VRN1TV4, 269XH13919, 1C89KKC04E, E4GA8884NN, 27YLU75U4W, R16CO5Y76E, G59M7S0WS3, 1Y17CTI5SR, 2BMD2GNA4V, 6RV024OAUQ, Q40Q9N063P, 8SKN0B0MIM, LKG8494WBH, R57ZHV85D4, 4R7X1O2820, 883WKN7W8X, 3T8H1794QW, 2DI9HA706A, 8CRQ2TH63M, 3B8D35Y7S4, 1VPU26JZZ4, 4T6H12BN9U, GN5P7K3T8S, 2P299V784P, YUL4LO94HK, O414PZ4LPZ, 2KR89I4H1Y, 506T60A25R, VCQ006KQ1E, K0U68Q2TXAUPC 0363113700770
Pharmacologic class: Adrenocorticotropic Hormone; Corticosteroid; Insulin; Mood Stabilizer; Nitrate Vasodilator; Nitrogen Binding Agent; Non-Standardized Chemical Allergen; Non-Standardized Plant Allergenic Extract; Nonsteroidal Anti-inflammatory Drug; Pediculicide; Platelet Aggregation Inhibitor; Standardized Chemical Allergen

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

N444911055601 followed by a unit qualifier and the quantity

Package 44911-0556-01. 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 weakness and exhaustion, minor abdominal cramps, bloating, and vomiting.** **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)