What is NDC 43742-0944?

43742-0944 is the product NDC for Oratox, Fucus vesiculosus 3 [hp_X]/mL + 23 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Oratox (Fucus Vesiculosus, Lymph Node (Suis), Medulla Ossis Suis, Thymus (Suis), Thyroidinum (Suis), Calcarea Muriatica, Iodium, Natrum Fluoratum, Natrum Muriaticum, Selenium Metallicum, Vanadium Metallicum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum Metallicum, Niccolum Metallicum, Palladium Metallicum, Stannum Metallicum, Titanium Metallicum, Zincum Metallicum).

What is the active ingredient?

Fucus vesiculosus, Sus scrofa lymph, Sus scrofa bone marrow, Sus scrofa thymus, Thyroid, Calcium chloride, Iodine, Sodium fluoride, Sodium chloride, Selenium, Vanadium, Silver, Gold, Copper, Eugenol, Formaldehyde, Lidocaine, Mercurius solubilis, Molybdenum, Nickel, Palladium, Tin, Titanium, Zinc.

Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Oratox?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Oratox NDC 43742-0944 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-0944Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-0944Add 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
43742-0944-1	4374209440143742094401	30 mL in 1 BOTTLE, DROPPER (43742-0944-1)Marketed from Dec 27, 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): Oratox
Generic name (nonproprietary): fucus vesiculosus, lymph node (suis), medulla ossis suis, thymus (suis), thyroidinum (suis), calcarea muriatica, iodium, natrum fluoratum, natrum muriaticum, selenium metallicum, vanadium metallicum, argentum metallicum, aurum metallicum, cuprum metallicum, eugenol, formalinum, lidocaine, mercurius solubilis, molybdenum metallicum, niccolum metallicum, palladium metallicum, stannum metallicum, titanium metallicum, zincum metallicum
Active ingredients: Fucus vesiculosus — 3 [hp_X]/mLSus scrofa lymph — 8 [hp_X]/mLSus scrofa bone marrow — 8 [hp_X]/mLSus scrofa thymus — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLCalcium chloride — 12 [hp_X]/mLIodine — 12 [hp_X]/mLSodium fluoride — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLVanadium — 12 [hp_X]/mLSilver — 12 [hp_X]/mLGold — 12 [hp_X]/mLCopper — 12 [hp_X]/mLEugenol — 12 [hp_X]/mLFormaldehyde — 12 [hp_X]/mLLidocaine — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLMolybdenum — 12 [hp_X]/mLNickel — 12 [hp_X]/mLPalladium — 12 [hp_X]/mLTin — 12 [hp_X]/mLTitanium — 12 [hp_X]/mLZinc — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.NDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 27, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Amides (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Local Anesthesia (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 43742-0944_f735ac6a-9396-4f30-8139-8afbaf56c87fSPL ID f735ac6a-9396-4f30-8139-8afbaf56c87fSPL set ID b78d8991-ffbe-4b11-b9b9-8fe432bed8aaUNII 535G2ABX9M, 33A7VYU29L, VP2CN2G7Y8, 7B69B0BD62, 6RV024OAUQ, M4I0D6VV5M, 9679TC07X4, 8ZYQ1474W7, 451W47IQ8X, H6241UJ22B, 00J9J9XKDE, 3M4G523W1G, 79Y1949PYO, 789U1901C5, 3T8H1794QW, 1HG84L3525, 98PI200987, 324Y4038G2, 81AH48963U, 7OV03QG267, 5TWQ1V240M, 387GMG9FH5, D1JT611TNE, J41CSQ7QDSUPC 0810151880679
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic; Blood Coagulation Factor; Copper-containing Intrauterine Device; Phosphate Binder; 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

N443742094401 followed by a unit qualifier and the quantity

Package 43742-0944-01. 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 23, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • muscle cramps • inflammation • joint pain These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43742-0944

What is NDC 43742-0944?: 43742-0944 is the product NDC for Oratox, Fucus vesiculosus 3 [hp_X]/mL + 23 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Oratox (Fucus Vesiculosus, Lymph Node (Suis), Medulla Ossis Suis, Thymus (Suis), Thyroidinum (Suis), Calcarea Muriatica, Iodium, Natrum Fluoratum, Natrum Muriaticum, Selenium Metallicum, Vanadium Metallicum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum Metallicum, Niccolum Metallicum, Palladium Metallicum, Stannum Metallicum, Titanium Metallicum, Zincum Metallicum).
What is the active ingredient?: Fucus vesiculosus, Sus scrofa lymph, Sus scrofa bone marrow, Sus scrofa thymus, Thyroid, Calcium chloride, Iodine, Sodium fluoride, Sodium chloride, Selenium, Vanadium, Silver, Gold, Copper, Eugenol, Formaldehyde, Lidocaine, Mercurius solubilis, Molybdenum, Nickel, Palladium, Tin, Titanium, Zinc.
Who is the labeler?: Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oratox?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.