Upper Resp HP NDC 44911-0595

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0595Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0595Add 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
44911-0595-1	44911059501	30 mL in 1 BOTTLE, DROPPER (44911-0595-1)Marketed from Jan 4, 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): Upper Resp HP
Generic name (nonproprietary): carbo vegetabilis, cuprum metallicum, drosera (rotundifolia), hepar sulphuris calcareum, ipecacuanha, lachesis mutus, lobelia inflata, phosphorus, pulsatilla (pratensis), rumex crispus, spongia tosta
Active ingredients: Activated charcoal — 30 [hp_X]/mLCopper — 30 [hp_X]/mLDrosera rotundifolia whole — 30 [hp_X]/mLCalcium sulfide — 30 [hp_X]/mLIpecac — 30 [hp_X]/mLLachesis muta venom — 30 [hp_X]/mLLobelia inflata whole — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLPulsatilla pratensis whole — 30 [hp_X]/mLRumex crispus root — 30 [hp_X]/mLSpongia officinalis skeleton, Roasted — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 4, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 44911-0595_95dcbcc9-a898-4bd2-92bc-a8d488664c15SPL ID 95dcbcc9-a898-4bd2-92bc-a8d488664c15SPL set ID a9c72c3a-908a-433b-ba9e-4f525b80ecaaUNII 2P3VWU3H10, 789U1901C5, QR44N9XPJQ, 1MBW07J51Q, 62I3C8233L, VSW71SS07I, 9PP1T3TC5U, 27YLU75U4W, 8E272251DI, 9N1RM2S62C, 1PIP394IID
Pharmacologic class: Copper-containing Intrauterine Device

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

N444911059501 followed by a unit qualifier and the quantity

Package 44911-0595-01. 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 31, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms of chronic cough, heaviness in chest, and bronchial irritation.** **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)