What is NDC 43742-1675?

43742-1675 is the product NDC for Dizzy, Sus scrofa cerebrum 6 [hp_X]/mL + 19 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?

Dizzy (Cerebellum (Suis), Bryonia (Alba), Petroleum, Tabacum, Ambra Grisea, Cyclamen Europaeum, Natrum Salicylicum, Argentum Nitricum, Asarum Canadense, Calcarea Sulphurica, Carboneum Sulphuratum, Chininum Sulphuricum, Cocculus Indicus, Conium Maculatum, Digitalis Purpurea, Gelsemium Sempervirens, Phosphorus, Piper Methysticum, Silicea, Theridion).

What is the active ingredient?

Sus scrofa cerebrum, Bryonia alba root, Kerosene, Tobacco leaf, Ambergris, Cyclamen purpurascens tuber, Sodium salicylate, Silver nitrate, Asarum canadense root, Calcium sulfate anhydrous, Carbon disulfide, Quinine sulfate, Anamirta cocculus seed, Conium maculatum flowering top, Digitalis, Gelsemium sempervirens root, Phosphorus, Macropiper methysticum root, Silicon dioxide, Theridion curassavicum.

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 Dizzy?

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.

Dizzy NDC 43742-1675 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1675Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1675Add 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
43742-1675-1	4374216750143742167501	30 mL in 1 BOTTLE, DROPPER (43742-1675-1)Marketed from Sep 22, 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): Dizzy
Generic name (nonproprietary): cerebellum (suis), bryonia (alba), petroleum, tabacum, ambra grisea, cyclamen europaeum, natrum salicylicum, argentum nitricum, asarum canadense, calcarea sulphurica, carboneum sulphuratum, chininum sulphuricum, cocculus indicus, conium maculatum, digitalis purpurea, gelsemium sempervirens, phosphorus, piper methysticum, silicea, theridion
Active ingredients: Sus scrofa cerebrum — 6 [hp_X]/mLBryonia alba root — 8 [hp_X]/mLKerosene — 8 [hp_X]/mLTobacco leaf — 8 [hp_X]/mLAmbergris — 9 [hp_X]/mLCyclamen purpurascens tuber — 9 [hp_X]/mLSodium salicylate — 10 [hp_X]/mLSilver nitrate — 12 [hp_X]/mLAsarum canadense root — 12 [hp_X]/mLCalcium sulfate anhydrous — 12 [hp_X]/mLCarbon disulfide — 12 [hp_X]/mLQuinine sulfate — 12 [hp_X]/mLAnamirta cocculus seed — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLDigitalis — 12 [hp_X]/mLGelsemium sempervirens root — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLMacropiper methysticum root — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLTheridion curassavicum — 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: Sep 22, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Phosphate Chelating Activity (Mechanism)Plant Proteins (Chemical structure)
Identifiers: Product ID 43742-1675_7581a689-8459-41c1-8546-c99d733347adSPL ID 7581a689-8459-41c1-8546-c99d733347adSPL set ID fdf934f8-7b12-4076-b8fb-00c095940697UNII 4GB5DQR532, T7J046YI2B, 1C89KKC04E, 6YR2608RSU, XTC0D02P6C, G728143D8Q, WIQ1H85SYP, 95IT3W8JZE, E2O4O7TQYK, E934B3V59H, S54S8B99E8, KF7Z0E0Q2B, 810258W28U, Q28R5GF371, F1T8QT9U8B, 639KR60Q1Q, 27YLU75U4W, BOW48C81XP, ETJ7Z6XBU4, 9Z8D3HEM8LUPC 0810151882130
Pharmacologic class: Antimalarial; Blood Coagulation Factor; Non-Standardized Plant Allergenic Extract; Phosphate Binder

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

N443742167501 followed by a unit qualifier and the quantity

Package 43742-1675-01. 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 Mar 15, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • vertigo • faintness • vomiting • motion sickness • spinning or swaying • weakness 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 43742-1675

What is NDC 43742-1675?: 43742-1675 is the product NDC for Dizzy, Sus scrofa cerebrum 6 [hp_X]/mL + 19 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?: Dizzy (Cerebellum (Suis), Bryonia (Alba), Petroleum, Tabacum, Ambra Grisea, Cyclamen Europaeum, Natrum Salicylicum, Argentum Nitricum, Asarum Canadense, Calcarea Sulphurica, Carboneum Sulphuratum, Chininum Sulphuricum, Cocculus Indicus, Conium Maculatum, Digitalis Purpurea, Gelsemium Sempervirens, Phosphorus, Piper Methysticum, Silicea, Theridion).
What is the active ingredient?: Sus scrofa cerebrum, Bryonia alba root, Kerosene, Tobacco leaf, Ambergris, Cyclamen purpurascens tuber, Sodium salicylate, Silver nitrate, Asarum canadense root, Calcium sulfate anhydrous, Carbon disulfide, Quinine sulfate, Anamirta cocculus seed, Conium maculatum flowering top, Digitalis, Gelsemium sempervirens root, Phosphorus, Macropiper methysticum root, Silicon dioxide, Theridion curassavicum.
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 Dizzy?: 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.