Homeoplex D NDC 71781-0003

NDC codes

FDA NDC Directory

Product NDC (as listed)71781-0003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71781-0003Add 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
71781-0003-1	71781000301	60 mL in 1 BOTTLE, DROPPER (71781-0003-1)Marketed from Nov 1, 2017

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): Homeoplex D
Generic name (nonproprietary): glycerinum, phytolacca decandra, taraxacum officinale, arsenicum album, nitricum acidum, nux vomica, petroleum, phosphoricum acidum, phosphorus, acetylsalicylicum acidum, glonoinum, insulinum (suis), lithium carbonicum, thyroidinum (suis), salicylicum acidum, adrenocorticotrophin, cortisone aceticum, eugenol, stearyl alcohol, xylitol, folliculinum, benzoicum acidum, chlorinum, potassium sorbate, sorbitol, resorcinum, benzyl alcohol, lacticum acidum, isopropyl palmitate, boricum acidum, aceticum acidum,
Active ingredients: Glycerin — 3 [hp_X]/mLPhytolacca americana root — 3 [hp_X]/mLTaraxacum officinale — 3 [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 pork — 12 [hp_X]/mLLithium carbonate — 12 [hp_X]/mLSus scrofa thyroid — 12 [hp_X]/mLSalicylic acid — 12 [hp_X]/mLCorticotropin — 12 [hp_X]/mLCortisone acetate — 12 [hp_X]/mLEugenol — 12 [hp_X]/mLStearyl alcohol — 12 [hp_X]/mLXylitol — 12 [hp_X]/mLEstrone — 12 [hp_X]/mLBenzoic acid — 12 [hp_X]/mLChlorine — 12 [hp_X]/mLPotassium sorbate — 12 [hp_X]/mLSorbitol — 12 [hp_X]/mLResorcinol — 12 [hp_X]/mLBenzyl alcohol — 12 [hp_X]/mLLactic acid, Dl- — 12 [hp_X]/mLIsopropyl palmitate — 12 [hp_X]/mLBoric acid — 12 [hp_X]/mLAcetic acid — 12 [hp_X]/mLPhenylbutazone — 12 [hp_X]/mLPetrolatum — 12 [hp_X]/mLLead — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Supplement Clinic, LLC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 1, 2017
Listing expires: Dec 31, 2026
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)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 71781-0003_b4f1a644-707b-4b5f-b9ae-355e323183b8SPL ID b4f1a644-707b-4b5f-b9ae-355e323183b8SPL set ID cd6b48ab-3566-484d-8deb-15ef6f8e7e8fUNII PDC6A3C0OX, 11E6VI8VEG, 39981FM375, S7V92P67HO, 411VRN1TV4, 269XH13919, 1C89KKC04E, E4GA8884NN, 27YLU75U4W, R16CO5Y76E, G59M7S0WS3, AVT680JB39, 2BMD2GNA4V, 6RV024OAUQ, O414PZ4LPZ, K0U68Q2TXA, 883WKN7W8X, 3T8H1794QW, 2KR89I4H1Y, VCQ006KQ1E, 2DI9HA706A, 8SKN0B0MIM, 4R7X1O2820, 1VPU26JZZ4, 506T60A25R, YUL4LO94HK, LKG8494WBH, 3B8D35Y7S4, 8CRQ2TH63M, R57ZHV85D4, Q40Q9N063P, GN5P7K3T8S, 4T6H12BN9U, 2P299V784PUPC 0799861441182
Pharmacologic class: Adrenocorticotropic Hormone; Corticosteroid; 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

N471781000301 followed by a unit qualifier and the quantity

Package 71781-0003-01. 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 Nov 1, 2017.

Indications (excerpt from the label)

INDICATIONS: For support of body's elimination systems.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)